A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930191



Internal ID22705454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11959808..11960099hg38UCSC Ensembl
chr18:11959807..11960098hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930191
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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