A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754505



Internal ID20530365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30556875..30556875hg38UCSC Ensembl
chr19:31047782..31047782hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284942
Samples
Known GenesZNF536
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754505
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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