A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028265



Internal ID21937608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76375666..76375767hg38UCSC Ensembl
chr18:74087621..74087722hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622364
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028265
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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