A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365928



Internal ID21023481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4851419..4876769hg38UCSC Ensembl
chr3:4893103..4918453hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3825351
hg1925351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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