A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365231



Internal ID21022784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53057798..53061191hg38UCSC Ensembl
chr3:53091814..53095207hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg383394
hg193394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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