A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477774



Internal ID22535675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:188332..189707hg38UCSC Ensembl
chr18:188332..189707hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874347
Supporting Variants
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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