A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482506



Internal ID21140059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37086144..37201353hg38UCSC Ensembl
chr14:37555349..37670558hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38115210
hg19115210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180094
Samples
Known GenesMIPOL1, SLC25A21, SLC25A21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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