A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365659



Internal ID21023212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107926101..107930000hg38UCSC Ensembl
chr3:107644948..107648847hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207209
Samples
Known GenesLINC00636
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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