A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873302



Internal ID22648247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:183609..185456hg38UCSC Ensembl
chr18:183609..185456hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381848
hg191848
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477773
Samples
Known GenesUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873302
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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