A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371295



Internal ID21028848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69075501..69082700hg38UCSC Ensembl
chr3:69124652..69131851hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211219
Samples
Known GenesUBA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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