A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581177



Internal ID16021900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23385552..23386793hg38UCSC Ensembl
Innerchr2:23608423..23609664hg19UCSC Ensembl
Innerchr2:23461928..23463169hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg381242
hg191242
hg181242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv904436
Samples
Known GenesKLHL29
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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