A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339508



Internal ID20997061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195610349..195618987hg38UCSC Ensembl
chr2:196475073..196483711hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg388639
hg198639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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