A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112077



Internal ID22021311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18027976..18027976hg38UCSC Ensembl
chr21:19400294..19400294hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647070
Samples
Known GenesCHODL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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