A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933614



Internal ID15880884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230699911..230801231hg38UCSC Ensembl
Innerchr2:231564626..231665946hg19UCSC Ensembl
Innerchr2:231272870..231374190hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38101321
hg19101321
hg18101321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584675
Supporting Variants
Samples
Known GenesCAB39, LOC151475
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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