A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569794



Internal ID16357203
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 StatusM
Merged Variants
Supporting Variantsnssv844318
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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