A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838769



Internal ID16132725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25086971..25088718hg38UCSC Ensembl
Innerchr15:25332118..25333865hg19UCSC Ensembl
Innerchr15:22883211..22884958hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381748
hg191748
hg181748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568535
Supporting Variants
Samples
Known GenesSNORD116-20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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