A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705600



Internal ID15442252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:157397389..157417146hg38UCSC Ensembl
Innerchr1:157367179..157386936hg19UCSC Ensembl
Innerchr1:155633803..155653560hg18UCSC Ensembl
Innerchr1:154180252..154200009hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3819758
hg1919758
hg1819758
hg1719758
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528914
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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