A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515112



Internal ID20888470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53380621..53494831hg38UCSC Ensembl
chr15:53672818..53787028hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38114211
hg19114211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025982
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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