A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370036



Internal ID21027589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29031543..29235593hg38UCSC Ensembl
chr3:29073034..29277084hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38204051
hg19204051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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