A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368230



Internal ID21025783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131361340..131381055hg38UCSC Ensembl
chr3:131080184..131099899hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3819716
hg1919716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208961
Samples
Known GenesLOC339874, NUDT16P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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