A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613939



Internal ID16401348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26641559..26691670hg38UCSC Ensembl
Innerchr9:26641557..26691668hg19UCSC Ensembl
Innerchr9:26631557..26681668hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3850112
hg1950112
hg1850112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12619n54
Supporting Variantsnssv1156744
SamplesHGDP01336
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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