A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357735



Internal ID21015288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53237744..53242384hg38UCSC Ensembl
chr3:53271760..53276400hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg384641
hg194641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101005
Samples
Known GenesTKT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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