A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933763



Internal ID22709079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113919871..113920251hg38UCSC Ensembl
chr13:114622844..114623224hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386208
Samples
Known GenesLINC00452
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933763
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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