A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371889



Internal ID21029442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37901257..37912062hg38UCSC Ensembl
chr3:37942748..37953553hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3810806
hg1910806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102169
Samples
Known GenesCTDSPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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