A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184526



Internal ID21323335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63091750..63091750hg38UCSC Ensembl
chr18:60758983..60758983hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926730
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184526
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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