A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377359



Internal ID22435229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22406150..22414279hg38UCSC Ensembl
chr18:19986113..19994242hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388130
hg198130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934536
Supporting Variants
Samples
Known GenesCTAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377359
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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