A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385396



Internal ID22443266
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 StatusS
Merged Variantsnsv5936639
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385396
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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