A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581689



Internal ID16369098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44240247..44241164hg38UCSC Ensembl
Innerchr2:44467386..44468303hg19UCSC Ensembl
Innerchr2:44320890..44321807hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38918
hg19918
hg18918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6836n54
Supporting Variantsnssv907985, nssv907986
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581689
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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