A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484317



Internal ID21141870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57546464..57714610hg38UCSC Ensembl
chr13:58120598..58288744hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38168147
hg19168147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011426
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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