A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178128



Internal ID21316924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63559526..63559786hg38UCSC Ensembl
chr20:62190879..62191139hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953961
Supporting Variants
SamplesHG002
Known GenesHELZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178128
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer