A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142732



Internal ID341933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128612241..128617520hg38UCSC Ensembl
chr8:129624487..129629766hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg385280
hg195280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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