A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482033



Internal ID21139586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96947487..97018801hg38UCSC Ensembl
chr13:97599741..97671055hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3871315
hg1971315
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184188
Samples
Known GenesLINC00359, OXGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482033
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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