A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614881



Internal ID16402290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93706793..93708566hg38UCSC Ensembl
Innerchr9:96469075..96470848hg19UCSC Ensembl
Innerchr9:95508896..95510669hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381774
hg191774
hg181774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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