A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705563



Internal ID15442215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110817180..110836356hg38UCSC Ensembl
Innerchr1:111359802..111378978hg19UCSC Ensembl
Innerchr1:111161325..111180501hg18UCSC Ensembl
Innerchr1:111071844..111091020hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819177
hg1919177
hg1819177
hg1719177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517082
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705563
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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