A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150977



Internal ID15508379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18237846..18282481hg38UCSC Ensembl
Innerchr21:19610163..19654798hg19UCSC Ensembl
Innerchr21:18532034..18576669hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3844636
hg1944636
hg1844636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587137
Supporting Variants
Samples1780862432_A
Known GenesCHODL, TMPRSS15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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