A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584905



Internal ID16372314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923589..240924528hg38UCSC Ensembl
Innerchr2:241863006..241863945hg19UCSC Ensembl
Innerchr2:241511679..241512618hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38940
hg19940
hg18940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7379n54
Supporting Variantsnssv934439, nssv934438
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584905
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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