A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360262



Internal ID21017815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68795110..68935519hg38UCSC Ensembl
chr3:68844261..68984670hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38140410
hg19140410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211215
Samples
Known GenesFAM19A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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