A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581549



Internal ID16368958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41003158..41035363hg38UCSC Ensembl
Innerchr2:41230298..41262503hg19UCSC Ensembl
Innerchr2:41083802..41116007hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3832206
hg1932206
hg1832206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6808n54
Supporting Variantsnssv906969, nssv906968, nssv906970
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581549
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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