A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767443



Internal ID20543303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33169674..33169674hg38UCSC Ensembl
chr19:33660580..33660580hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291841
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767443
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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