A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363191



Internal ID21020744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132534899..132535359hg38UCSC Ensembl
chr3:132253743..132254203hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094175
Samples
Known GenesDNAJC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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