A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943963



Internal ID22719420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55989536..55997434hg38UCSC Ensembl
chr18:53656767..53664665hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg387899
hg197899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943963
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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