A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613687



Internal ID16401096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16937554..16982586hg38UCSC Ensembl
Innerchr9:16937552..16982584hg19UCSC Ensembl
Innerchr9:16927552..16972584hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3845033
hg1945033
hg1845033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12580n54
Supporting Variantsnssv1156255
Samples1782681313_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613687
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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