A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178093



Internal ID21316889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34528006..34528339hg38UCSC Ensembl
chr20:33115811..33116144hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943768
Supporting Variants
SamplesHG002
Known GenesDYNLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178093
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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