A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839799



Internal ID16133755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33883771..33902385hg38UCSC Ensembl
Innerchr15:34175972..34194586hg19UCSC Ensembl
Innerchr15:31963264..31981878hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3818615
hg1918615
hg1818615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568922
Supporting Variants
Samples
Known GenesAVEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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