A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941953



Internal ID22717384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76052485..76054136hg38UCSC Ensembl
chr18:73764440..73766091hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381652
hg191652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17406806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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