A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581173



Internal ID16021896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23376693..23435745hg38UCSC Ensembl
Innerchr2:23599564..23658616hg19UCSC Ensembl
Innerchr2:23453069..23512121hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3859053
hg1959053
hg1859053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904431
Samples
Known GenesKLHL29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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