A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021619



Internal ID22083250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76303839..76318064hg38UCSC Ensembl
Outerchr6:76294154..76323236hg38UCSC Ensembl
Innerchr6:77013556..77027781hg19UCSC Ensembl
Outerchr6:77003871..77032953hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3829083
hg1929083
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156531
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021619
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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