A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858032



Internal ID22632967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91191014..91216056hg38UCSC Ensembl
chr13:91843268..91868310hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3825043
hg1925043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463606
Samples
Known GenesLINC00379
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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