A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349680



Internal ID21007233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135184589..135184965hg38UCSC Ensembl
chr2:135942159..135942535hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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