A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614785



Internal ID16402194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87055090..87162582hg38UCSC Ensembl
Innerchr9:89670005..89777497hg19UCSC Ensembl
Innerchr9:88859825..88967317hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38107493
hg19107493
hg18107493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176362
SamplesHGDP00955
Known GenesC9orf170, LOC494127
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614785
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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