A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352133



Internal ID21009686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70293977..70294588hg38UCSC Ensembl
chr2:70521109..70521720hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352133
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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