A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv720716



Internal ID16014672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106737267..106951642hg38UCSC Ensembl
Innerchr1:107279889..107494264hg19UCSC Ensembl
Innerchr1:107081412..107295787hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38214376
hg19214376
hg18214376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547329
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)nssv720716
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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