A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1124236



Internal ID15630736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139658470..139701654hg38UCSC Ensembl
Innerchr8:140670713..140713897hg19UCSC Ensembl
Innerchr8:140739895..140783079hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3843185
hg1943185
hg1843185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612541
Supporting Variants
Samples
Known GenesKCNK9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1124236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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