A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361210



Internal ID21018763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3988052..4076397hg38UCSC Ensembl
chr3:4029736..4118081hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3888346
hg1988346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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