A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479186



Internal ID22537088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63512712..63523592hg38UCSC Ensembl
chr18:61179945..61190825hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3810881
hg1910881
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479186
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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