A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363796



Internal ID21021349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53327530..53327863hg38UCSC Ensembl
chr3:53361557..53361890hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101012
Samples
Known GenesDCP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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