A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584793



Internal ID16372202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239400958..239401522hg38UCSC Ensembl
Innerchr2:240322652..240323216hg19UCSC Ensembl
Innerchr2:239987589..239988153hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38565
hg19565
hg18565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933816
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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