A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482102



Internal ID21139655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20825574..20826124hg38UCSC Ensembl
chr13:21399713..21400263hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007689
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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