A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357374



Internal ID21014927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37990021..37996235hg38UCSC Ensembl
chr3:38031512..38037726hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386215
hg196215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102177
Samples
Known GenesVILL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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