A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142703



Internal ID341904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94923819..94923910hg38UCSC Ensembl
chr8:95936047..95936138hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142703
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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