A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145636



Internal ID20712676
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 StatusS
Merged Variantsnsv6398451
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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