A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478500



Internal ID22536401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4684971..4689884hg38UCSC Ensembl
chr18:4684971..4689884hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478500
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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