A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939080



Internal ID22714469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77726505..77734272hg38UCSC Ensembl
chr18:75438461..75446228hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg387768
hg197768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939080
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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