A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839596



Internal ID16133552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483297..31484086hg38UCSC Ensembl
Innerchr15:31775500..31776289hg19UCSC Ensembl
Innerchr15:29562792..29563581hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38790
hg19790
hg18790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568809
Supporting Variants
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839596
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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