A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363972



Internal ID21021525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100610201..100718500hg38UCSC Ensembl
chr3:100329045..100437344hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38108300
hg19108300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4953n223
Supporting Variantsnssv18208858
Samples
Known GenesGPR128, TFG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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