A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933819



Internal ID16227775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239704749..239748351hg38UCSC Ensembl
Innerchr2:240626443..240670045hg19UCSC Ensembl
Innerchr2:240291380..240334982hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3843603
hg1943603
hg1843603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584797
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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