A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903829



Internal ID16197785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14226572..14450758hg38UCSC Ensembl
Innerchr2:14366696..14590882hg19UCSC Ensembl
Innerchr2:14284147..14508333hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38224187
hg19224187
hg18224187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581023
Supporting Variants
Samples
Known GenesLINC00276
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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