A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368473



Internal ID21026026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83573753..83820452hg38UCSC Ensembl
chr3:83622904..83869603hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38246700
hg19246700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368473
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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