A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370913



Internal ID21028466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58502340..60224074hg38UCSC Ensembl
chr3:58488067..60209802hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381721735
hg191721736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212293
Samples
Known GenesACOX2, C3orf67, FAM107A, FAM3D, FHIT, KCTD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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