A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710222



Internal ID16004178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13118218..13151495hg38UCSC Ensembl
Innerchr1:13185690..13218946hg19UCSC Ensembl
Innerchr1:13108277..13141533hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3833278
hg1933257
hg1833257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545545
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)nssv710222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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