A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv843013



Internal ID16136969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52709341..52746291hg38UCSC Ensembl
Innerchr15:53001538..53038488hg19UCSC Ensembl
Innerchr15:50788830..50825780hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3836951
hg1936951
hg1836951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569425
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)nssv843013
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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