A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048471



Internal ID21957704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51785186..51785241hg38UCSC Ensembl
chr20:50401725..50401780hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631485
Samples
Known GenesSALL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048471
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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