A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653765



Internal ID15043731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77308728..77312923hg38UCSC Ensembl
Innerchr1:77774413..77778608hg19UCSC Ensembl
Innerchr1:77547001..77551196hg18UCSC Ensembl
Innerchr1:77486434..77490629hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384196
hg194196
hg184196
hg174196
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517088
Supporting Variants
Samples
Known GenesAK5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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