A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584798



Internal ID16372207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239705056..239748351hg38UCSC Ensembl
Innerchr2:240626750..240670045hg19UCSC Ensembl
Innerchr2:240291687..240334982hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3843296
hg1943296
hg1843296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7358n54
Supporting Variantsnssv1151184
Samples1780862573_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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