A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339773



Internal ID20997326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19483348..20077709hg38UCSC Ensembl
chr2:19683109..20277470hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38594362
hg19594362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3804n223
Supporting Variantsnssv18206092
Samples
Known GenesLAPTM4A, LINC00954, MATN3, TTC32, WDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339773
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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