A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189020



Internal ID21327862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59355821..59355821hg38UCSC Ensembl
chr20:57930876..57930876hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944805
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189020
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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