A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929111



Internal ID22704360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6651748..6678479hg38UCSC Ensembl
chr18:6651747..6678478hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3826732
hg1926732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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