A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028965



Internal ID21938308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68964425..68964552hg38UCSC Ensembl
chr15:69256764..69256891hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602023
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028965
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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