A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982135



Internal ID15929405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178832458..178832742hg38UCSC Ensembl
Innerchr3:178550246..178550530hg19UCSC Ensembl
Innerchr3:180032940..180033224hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38285
hg19285
hg18285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592641
Supporting Variants
Samples
Known GenesKCNMB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982135
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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