A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020158



Internal ID22081789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12791219..12795017hg38UCSC Ensembl
Outerchr8:12788880..12796024hg38UCSC Ensembl
Innerchr8:12648728..12652526hg19UCSC Ensembl
Outerchr8:12646389..12653533hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg387145
hg197145
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156864
Supporting Variants
Samples
Known GenesLINC00681, LOC340357
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020158
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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