A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354667



Internal ID21012220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62645307..62648653hg38UCSC Ensembl
chr2:62872442..62875788hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383347
hg193347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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