A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350834



Internal ID21008387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:120568863..120647513hg38UCSC Ensembl
chr2:121326439..121405089hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3878651
hg1978651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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