A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186326



Internal ID21325140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17778562..17778562hg38UCSC Ensembl
chr20:17759207..17759207hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945016
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186326
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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