A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497695



Internal ID20870903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66299495..66299958hg38UCSC Ensembl
chr15:66591833..66592296hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025403
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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