A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029488



Internal ID21938831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76966978..76967410hg38UCSC Ensembl
chr18:74678934..74679366hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628383
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029488
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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