A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034420



Internal ID21943763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14112045..14112112hg38UCSC Ensembl
chr18:14112044..14112111hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622798
Samples
Known GenesZNF519
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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