A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075869



Internal ID21985102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189961594..189961594hg38UCSC Ensembl
chr3:189679383..189679383hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545155
Samples
Known GenesLEPREL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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