A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146687



Internal ID345892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8522360..8706540hg38UCSC Ensembl
chr21:9411194..9595373hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38184181
hg19184180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146687
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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