A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471374



Internal ID22529265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57732709..57744001hg38UCSC Ensembl
chr18:55399941..55411233hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3811293
hg1911293
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878423
Supporting Variants
Samples
Known GenesATP8B1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471374
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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