A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478444



Internal ID22536345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40225621..40227820hg38UCSC Ensembl
chr18:37805585..37807784hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478444
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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