A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381945



Internal ID22439815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60191130..60191130hg38UCSC Ensembl
chr18:57858363..57858363hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381945
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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