A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904886



Internal ID15852156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33000138..33001706hg38UCSC Ensembl
Innerchr2:33225205..33226773hg19UCSC Ensembl
Innerchr2:33078709..33080277hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381569
hg191569
hg181569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581304
Supporting Variants
Samples
Known GenesLTBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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