A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv717750



Internal ID16011706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79519063..79694284hg38UCSC Ensembl
Innerchr1:79984748..80159969hg19UCSC Ensembl
Innerchr1:79757336..79932557hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38175222
hg19175222
hg18175222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546637
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv717750
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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