A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614876



Internal ID16402285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91640140..91641031hg38UCSC Ensembl
Innerchr9:94402422..94403313hg19UCSC Ensembl
Innerchr9:93442243..93443134hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38892
hg19892
hg18892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12794n54
Supporting Variantsnssv1139364
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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