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dbVar

Database of genomic structural variation

nsv6635964

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:83,835

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: 297 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):116,316,286-116,400,120

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635964	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	116,316,286	116,400,120
nsv6635964	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	118,075,798	118,159,632

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18327042	duplication	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
nssv18327042	Remapped	Perfect	NC_000010.11:g.(11 6316286_?)_(?_1164 00120)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	116,316,286	116,400,120
nssv18327042	Submitted genomic		NC_000010.10:g.(11 8075798_?)_(?_1181 59632)dup	GRCh37 (hg19)		NC_000010.10	Chr10	118,075,798	118,159,632

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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