A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372179



Internal ID21029732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18940404..18943675hg38UCSC Ensembl
chr3:18981896..18985167hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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