A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585006



Internal ID16372415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241915920..242060570hg38UCSC Ensembl
Innerchr2:242858071..243002721hg19UCSC Ensembl
Innerchr2:242506744..242651394hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38144651
hg19144651
hg18144651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7399n54
Supporting Variantsnssv934836
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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