A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936713



Internal ID22712071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63192970..63193108hg38UCSC Ensembl
chr15:63485169..63485307hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377534
Samples
Known GenesRAB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936713
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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