A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844318



Internal ID16138274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66586562..66611228hg38UCSC Ensembl
Innerchr15:66878900..66903566hg19UCSC Ensembl
Innerchr15:64665954..64690620hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3824667
hg1924667
hg1824667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569794
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)nssv844318
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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