A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697864



Internal ID15434516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5223882..5227048hg38UCSC Ensembl
Innerchr1:5283942..5287108hg19UCSC Ensembl
Innerchr1:5183802..5186968hg18UCSC Ensembl
Innerchr1:5194315..5197481hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg383167
hg193167
hg183167
hg173167
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521242
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697864
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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