A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664272



Internal ID15054238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21813855..21873328hg38UCSC Ensembl
Innerchr1:22140348..22199821hg19UCSC Ensembl
Innerchr1:22012935..22072408hg18UCSC Ensembl
Innerchr1:21885654..21945127hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3859474
hg1959474
hg1859474
hg1759474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515659
Supporting Variants
Samples
Known GenesHSPG2, LDLRAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664272
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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