A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705759



Internal ID15095725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21831870..21851385hg38UCSC Ensembl
Innerchr1:22158363..22177878hg19UCSC Ensembl
Innerchr1:22030950..22050465hg18UCSC Ensembl
Innerchr1:21903669..21923184hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3819516
hg1919516
hg1819516
hg1719516
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515659
Supporting Variants
Samples
Known GenesHSPG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705759
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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