A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584906



Internal ID16372315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923589..240924590hg38UCSC Ensembl
Innerchr2:241863006..241864007hg19UCSC Ensembl
Innerchr2:241511679..241512680hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381002
hg191002
hg181002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7379n54
Supporting Variantsnssv934440, nssv934441
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584906
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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