A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615521



Internal ID16056244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130283369..130309639hg38UCSC Ensembl
Innerchr9:133045648..133071918hg19UCSC Ensembl
Innerchr9:132085469..132111739hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3826271
hg1926271
hg1826271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176509
SamplesHGDP00049
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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