A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743016



Internal ID20519002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23375230..23375334hg38UCSC Ensembl
chr19:23558032..23558136hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286420
Samples
Known GenesZNF91
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743016
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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