A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614609



Internal ID16402018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71960265..72011980hg38UCSC Ensembl
Innerchr9:74575181..74626896hg19UCSC Ensembl
Innerchr9:73765001..73816716hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3851716
hg1951716
hg1851716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137199
Samples
Known GenesC9orf85
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614609
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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