A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349789



Internal ID21007342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13229618..13238698hg38UCSC Ensembl
chr2:13369743..13378823hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg389081
hg199081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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