A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705039



Internal ID15441691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110933131..110933219hg38UCSC Ensembl
Innerchr1:111475753..111475841hg19UCSC Ensembl
Innerchr1:111277276..111277364hg18UCSC Ensembl
Innerchr1:111187795..111187883hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3889
hg1989
hg1889
hg1789
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528444
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705039
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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