A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187720



Internal ID21326551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009487..11009487hg38UCSC Ensembl
chr20:10990135..10990135hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933700
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187720
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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