A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371858



Internal ID21029411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119672301..119679200hg38UCSC Ensembl
chr3:119391148..119398047hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207917
Samples
Known GenesCOX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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