A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206963



Internal ID20774003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66612182..66620498hg38UCSC Ensembl
chr2:66839314..66847630hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg388317
hg198317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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