A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv948121



Internal ID16242077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44199484..44208093hg38UCSC Ensembl
Innerchr21:45619367..45627976hg19UCSC Ensembl
Innerchr21:44443795..44452404hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg388610
hg198610
hg188610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587730
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv948121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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