A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587723



Internal ID16375132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44197445..44200822hg38UCSC Ensembl
Innerchr21:45617328..45620705hg19UCSC Ensembl
Innerchr21:44441756..44445133hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948049
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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