A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397668



Internal ID21055221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64790857..65165358hg38UCSC Ensembl
chr6:65500750..65875251hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38374502
hg19374502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6215n223
Supporting Variantsnssv18145623
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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