A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047681



Internal ID21956914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38407611..38409354hg38UCSC Ensembl
chr20:37036258..37038002hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381744
hg191745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047681
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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