A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189069



Internal ID21327919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63853700..63853700hg38UCSC Ensembl
chr20:62485053..62485053hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926227
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189069
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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