A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589855



Internal ID16377264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:19367661..19470582hg38UCSC Ensembl
Innerchr3:19409153..19512074hg19UCSC Ensembl
Innerchr3:19384157..19487078hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38102922
hg19102922
hg18102922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959876
Samples
Known GenesKCNH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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