A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929478



Internal ID22704732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24525945..24535941hg38UCSC Ensembl
chr18:22105909..22115905hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg389997
hg199997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929478
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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