A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504617



Internal ID20877879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58153771..58154452hg38UCSC Ensembl
chr15:58445970..58446651hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026147
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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