A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358932



Internal ID21016485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128943788..128944184hg38UCSC Ensembl
chr3:128662631..128663027hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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