A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699756



Internal ID15436408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:40011129..40033630hg38UCSC Ensembl
Innerchr1:40476801..40499302hg19UCSC Ensembl
Innerchr1:40249388..40271889hg18UCSC Ensembl
Innerchr1:40145894..40168395hg17UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3822502
hg1922502
hg1822502
hg1722502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523913
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699756
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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