A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584901



Internal ID16372310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923534..240933180hg38UCSC Ensembl
Innerchr2:241862951..241872597hg19UCSC Ensembl
Innerchr2:241511624..241521270hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg389647
hg199647
hg189647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7382n54
Supporting Variantsnssv934424
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584901
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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