A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047976



Internal ID21957209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50938830..50938887hg38UCSC Ensembl
chr20:49555367..49555424hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619466
Samples
Known GenesDPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047976
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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