A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398451



Internal ID21056004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64864405..65187430hg38UCSC Ensembl
chr6:65574298..65897323hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38323026
hg19323026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6215n223
Supporting Variantsnssv18145636
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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