A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614322



Internal ID16401731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66860632..67213019hg38UCSC Ensembl
Innerchr9:40479822..40832209hg19UCSC Ensembl
Innerchr9:40469822..40822209hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38352388
hg19352388
hg18352388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134152
Samples
Known GenesFAM74A3, SPATA31A3, ZNF658
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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