A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142135



Internal ID341335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23272374..23272460hg38UCSC Ensembl
chr8:23129887..23129973hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142135
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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