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dbVar

Database of genomic structural variation

nsv6635658

Organism: Homo sapiens

Study:nstd227 (Kikas et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:5
Validation:Not tested
Clinical Assertions: No
Region Size:174,844

Publication(s):Kikas et al. 2023

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: 1294 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):136,670,241-136,845,084

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635658	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nsv6635658	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	137,682,484	137,857,327

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18326786	deletion	SNP array	Probe signal intensity
nssv18326787	deletion	SNP array	Probe signal intensity
nssv18326788	deletion	SNP array	Probe signal intensity
nssv18326789	deletion	SNP array	Probe signal intensity
nssv18326790	deletion	SNP array	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18326786	Remapped	Perfect	NC_000008.11:g.(13 6670241_?)_(?_1368 45084)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nssv18326787	Remapped	Perfect	NC_000008.11:g.(13 6670241_?)_(?_1368 45084)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nssv18326788	Remapped	Perfect	NC_000008.11:g.(13 6670241_?)_(?_1368 45084)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nssv18326789	Remapped	Perfect	NC_000008.11:g.(13 6670241_?)_(?_1368 45084)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nssv18326790	Remapped	Perfect	NC_000008.11:g.(13 6670241_?)_(?_1368 45084)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,670,241	136,845,084
nssv18326786	Submitted genomic		NC_000008.10:g.(13 7682484_?)_(?_1378 57327)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,682,484	137,857,327
nssv18326787	Submitted genomic		NC_000008.10:g.(13 7682484_?)_(?_1378 57327)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,682,484	137,857,327
nssv18326788	Submitted genomic		NC_000008.10:g.(13 7682484_?)_(?_1378 57327)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,682,484	137,857,327
nssv18326789	Submitted genomic		NC_000008.10:g.(13 7682484_?)_(?_1378 57327)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,682,484	137,857,327
nssv18326790	Submitted genomic		NC_000008.10:g.(13 7682484_?)_(?_1378 57327)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,682,484	137,857,327

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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