A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507372



Internal ID20880662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84993181..84994704hg38UCSC Ensembl
chr15:85536412..85537935hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381524
hg191524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027243
Samples
Known GenesPDE8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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