A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933071



Internal ID22708379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34233869..34235305hg38UCSC Ensembl
chr18:31813833..31815269hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933071
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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