A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150983



Internal ID15880777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682124..18718761hg38UCSC Ensembl
Innerchr21:20054442..20091079hg19UCSC Ensembl
Innerchr21:18976313..19012950hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3836638
hg1936638
hg1836638
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587144
Supporting Variants
SamplesNINDS_271
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150983
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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