A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581109



Internal ID16368518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18004324..18070689hg38UCSC Ensembl
Innerchr2:18185590..18251955hg19UCSC Ensembl
Innerchr2:18049071..18115436hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3866366
hg1966366
hg1866366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6722n54
Supporting Variantsnssv1150407, nssv904163
SamplesHGDP00007
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581109
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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