A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360856



Internal ID21018409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126893389..126948469hg38UCSC Ensembl
chr3:126612232..126667312hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3855081
hg1955081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208470
Samples
Known GenesCHCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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