A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343820



Internal ID21001373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:35065514..35720591hg38UCSC Ensembl
chr2:35290580..35945657hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38655078
hg19655078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343820
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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