A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372929



Internal ID21030482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122200001..122204900hg38UCSC Ensembl
chr3:121918848..121923747hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207943
Samples
Known GenesCASR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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