A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587815



Internal ID16028538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44886246..44902938hg38UCSC Ensembl
Innerchr21:46306161..46322853hg19UCSC Ensembl
Innerchr21:45130589..45147281hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816693
hg1916693
hg1816693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7893n54
Supporting Variantsnssv1151415
SamplesHGDP00676
Known GenesITGB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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