A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367398



Internal ID21024951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81138452..81139098hg38UCSC Ensembl
chr3:81187603..81188249hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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