A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377131



Internal ID22435001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13656641..13658201hg38UCSC Ensembl
chr18:13656640..13658200hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377131
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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