A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142064



Internal ID341264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144767544..144768009hg38UCSC Ensembl
chr8:145992929..145993394hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17018471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142064
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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