A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592646



Internal ID16033369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178837810..178848654hg38UCSC Ensembl
Innerchr3:178555598..178566442hg19UCSC Ensembl
Innerchr3:180038292..180049136hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3810845
hg1910845
hg1810845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982506
Samples
Known GenesKCNMB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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