A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585019



Internal ID16372428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241925381..242082731hg38UCSC Ensembl
Innerchr2:242867532..243024882hg19UCSC Ensembl
Innerchr2:242516205..242673555hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38157351
hg19157351
hg18157351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7399n54
Supporting Variantsnssv934855
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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