A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936639



Internal ID22711996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53589334..53589629hg38UCSC Ensembl
chr18:51115704..51115999hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936639
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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