A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363543



Internal ID21021096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126826286..126831347hg38UCSC Ensembl
chr3:126545129..126550190hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg385062
hg195062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094075
Samples
Known GenesCHCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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