A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936630



Internal ID22711987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84226859..84234326hg38UCSC Ensembl
chr13:84800994..84808461hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg387468
hg197468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375610
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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