A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751859



Internal ID16045815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80453946..80460841hg38UCSC Ensembl
Innerchr10:82213702..82220597hg19UCSC Ensembl
Innerchr10:82203682..82210577hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386896
hg196896
hg186896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551641
Supporting Variants
Samples
Known GenesTSPAN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751859
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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