A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948068



Internal ID21368137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61229617..61229667hg38UCSC Ensembl
chr20:59804673..59804723hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179594
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948068
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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