A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343277



Internal ID21000830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70332540..70335283hg38UCSC Ensembl
chr2:70559672..70562415hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg382744
hg192744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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