A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371213



Internal ID21028766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119158601..119160600hg38UCSC Ensembl
chr3:118877448..118879447hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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