A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024193



Internal ID20591233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39884965..39887217hg38UCSC Ensembl
chr15:40177166..40179418hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499457
Supporting Variants
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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