A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366112



Internal ID21023665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56629029..56631839hg38UCSC Ensembl
chr3:56663057..56665867hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212269
Samples
Known GenesFAM208A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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