A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359148



Internal ID21016701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692401..107699500hg38UCSC Ensembl
chr3:107411248..107418347hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg387100
hg197100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4971n223
Supporting Variantsnssv18207206
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359148
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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