A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943719



Internal ID22719172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8934744..8934845hg38UCSC Ensembl
chr18:8934742..8934843hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943719
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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