A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354339



Internal ID21011892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206796501..206803000hg38UCSC Ensembl
chr2:207661225..207667724hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4268n223
Supporting Variantsnssv18208102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354339
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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