A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661821



Internal ID15051787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32874437..32912078hg38UCSC Ensembl
Innerchr1:33340038..33377679hg19UCSC Ensembl
Innerchr1:33112625..33150266hg18UCSC Ensembl
Innerchr1:33009131..33046772hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3837642
hg1937642
hg1837642
hg1737642
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516302
Supporting Variants
Samples
Known GenesHPCA, TMEM54
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661821
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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