A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705361



Internal ID15442013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95622636..95674464hg38UCSC Ensembl
Innerchr1:96088192..96140020hg19UCSC Ensembl
Innerchr1:95860780..95912608hg18UCSC Ensembl
Innerchr1:95800213..95852041hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3851829
hg1951829
hg1851829
hg1751829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528711
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705361
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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