A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939741



Internal ID22715139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89470539..89522530hg38UCSC Ensembl
chr15:90013770..90065761hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3851992
hg1951992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372905
Samples
Known GenesLINC00928, RHCG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939741
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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