A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982444



Internal ID15929714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178832458..178850341hg38UCSC Ensembl
Innerchr3:178550246..178568129hg19UCSC Ensembl
Innerchr3:180032940..180050823hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3817884
hg1917884
hg1817884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592645
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)nssv982444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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