A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722862



Internal ID146528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33158399..33171456hg38UCSC Ensembl
chr19:33649305..33662362hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3813058
hg1913058
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554846
Supporting Variants
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722862
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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