A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005047



Internal ID22066678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127673996..127678967hg38UCSC Ensembl
Outerchr8:127673137..127679774hg38UCSC Ensembl
Innerchr8:128686241..128691212hg19UCSC Ensembl
Outerchr8:128685382..128692019hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386638
hg196638
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154390
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005047
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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