A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021059



Internal ID21930402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3772083..3772387hg38UCSC Ensembl
chr18:3772083..3772387hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634297
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021059
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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