A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962459



Internal ID16256415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45507536..45510525hg38UCSC Ensembl
Innerchr3:45549028..45552017hg19UCSC Ensembl
Innerchr3:45524032..45527021hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382990
hg192990
hg182990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590166
Supporting Variants
Samples
Known GenesLARS2, LARS2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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