A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336212



Internal ID20993765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113083107..113089640hg38UCSC Ensembl
chr2:113840684..113847217hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg386534
hg196534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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