A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365519



Internal ID21023072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53300562..53309712hg38UCSC Ensembl
chr3:53334592..53343742hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg389151
hg199151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101010
Samples
Known GenesDCP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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