A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336713



Internal ID20994266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103303582..103323047hg38UCSC Ensembl
chr2:103920040..103939505hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3819466
hg1919466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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