A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477242



Internal ID22535143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:158021..162915hg38UCSC Ensembl
chr18:158021..162915hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg384895
hg194895
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874921
Supporting Variants
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477242
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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