A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478498



Internal ID22536399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4684250..4687609hg38UCSC Ensembl
chr18:4684250..4687609hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478498
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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