A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491083



Internal ID21148636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57696564..57697259hg38UCSC Ensembl
chr13:58270698..58271393hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011459
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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