A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359508



Internal ID21017061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58682168..58792751hg38UCSC Ensembl
chr3:58667895..58778478hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38110584
hg19110584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212296
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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