A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420716



Internal ID21078269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158832286..159197356hg38UCSC Ensembl
chr7:158624977..158990045hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38365071
hg19365069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7208n223
Supporting Variantsnssv18229252
Samples
Known GenesLINC00689, VIPR2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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