Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6635036

Organism: Homo sapiens

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

Variant Calls:4
Validation:Not tested
Clinical Assertions: No
Region Size:664

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

Remapped(Score: Perfect):17,723,282-17,723,945

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635036	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	17,723,282	17,723,945
nsv6635036	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	17,580,791	17,581,454

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18326778	deletion	SNP array	Probe signal intensity
nssv18326779	deletion	SNP array	Probe signal intensity
nssv18326780	deletion	SNP array	Probe signal intensity
nssv18328825	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
nssv18326778	Remapped	Perfect	NC_000008.11:g.(17 723282_?)_(?_17723 945)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	17,723,282	17,723,945
nssv18326779	Remapped	Perfect	NC_000008.11:g.(17 723282_?)_(?_17723 945)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	17,723,282	17,723,945
nssv18326780	Remapped	Perfect	NC_000008.11:g.(17 723282_?)_(?_17723 945)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	17,723,282	17,723,945
nssv18328825	Remapped	Perfect	NC_000008.11:g.(17 723282_?)_(?_17723 945)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	17,723,282	17,723,945
nssv18326778	Submitted genomic		NC_000008.10:g.(17 580791_?)_(?_17581 454)del	GRCh37 (hg19)		NC_000008.10	Chr8	17,580,791	17,581,454
nssv18326779	Submitted genomic		NC_000008.10:g.(17 580791_?)_(?_17581 454)del	GRCh37 (hg19)		NC_000008.10	Chr8	17,580,791	17,581,454
nssv18326780	Submitted genomic		NC_000008.10:g.(17 580791_?)_(?_17581 454)del	GRCh37 (hg19)		NC_000008.10	Chr8	17,580,791	17,581,454
nssv18328825	Submitted genomic		NC_000008.10:g.(17 580791_?)_(?_17581 454)del	GRCh37 (hg19)		NC_000008.10	Chr8	17,580,791	17,581,454

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

You are here: NCBI