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dbVar

Database of genomic structural variation

nsv7099302

Organism: Homo sapiens

Study:nstd231 (Ali et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:6
Validation:Not tested
Clinical Assertions: No
Region Size:33,991

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 465 SVs from 53 studies. See in: genome view

Remapped(Score: Perfect):155,683,281-155,717,271

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099302	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nsv7099302	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	154,912,942	154,946,932

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18792896	deletion	SNP array	SNP genotyping analysis
nssv18792928	deletion	SNP array	SNP genotyping analysis
nssv18792930	deletion	SNP array	SNP genotyping analysis
nssv18792932	deletion	SNP array	SNP genotyping analysis
nssv18792934	deletion	SNP array	SNP genotyping analysis
nssv18792935	deletion	SNP array	SNP genotyping analysis

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18792896	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792928	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792930	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792932	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792934	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792935	Remapped	Perfect	NC_000023.11:g.(15 5683281_?)_(?_1557 17271)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	155,683,281	155,717,271
nssv18792896	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932
nssv18792928	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932
nssv18792930	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932
nssv18792932	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932
nssv18792934	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932
nssv18792935	Submitted genomic		NC_000023.10:g.(15 4912942_?)_(?_1549 46932)del	GRCh37 (hg19)		NC_000023.10	ChrX	154,912,942	154,946,932

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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