A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488100



Internal ID21145653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113165956..113166562hg38UCSC Ensembl
chr13:113820270..113820876hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007319
Samples
Known GenesPROZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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