A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371060



Internal ID21028613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86171222..86174168hg38UCSC Ensembl
chr3:86220372..86223318hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg382947
hg192947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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