A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498615



Internal ID20871827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68988449..68996652hg38UCSC Ensembl
chr15:69280788..69288991hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388204
hg198204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026286
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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