A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150498



Internal ID15880738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:121059276..121099332hg38UCSC Ensembl
Innerchr2:121816852..121856908hg19UCSC Ensembl
Innerchr2:121533322..121573378hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3840057
hg1940057
hg1840057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582804
Supporting Variants
SamplesNINDS_259
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150498
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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