A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479160



Internal ID22537062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59547672..59550871hg38UCSC Ensembl
chr18:57214904..57218103hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875971
Supporting Variants
Samples
Known GenesCCBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479160
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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