A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372266



Internal ID21029819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69547629..69669121hg38UCSC Ensembl
chr3:69596780..69718272hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38121493
hg19121493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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