A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499457



Internal ID20872677
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 StatusM
Merged Variants
Supporting Variantsnssv18024193
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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