A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373326



Internal ID21030879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58425416..58428347hg38UCSC Ensembl
chr3:58411143..58414074hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382932
hg192932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102941
Samples
Known GenesPDHB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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