A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337640



Internal ID20995193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219196473..219202935hg38UCSC Ensembl
chr2:220061195..220067657hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386463
hg196463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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