A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851214



Internal ID15798484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101683568..101752560hg38UCSC Ensembl
Innerchr15:102223771..102292763hg19UCSC Ensembl
Innerchr15:100041294..100110286hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3868993
hg1968993
hg1868993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570909
Supporting Variants
Samples
Known GenesTARSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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