A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142338



Internal ID341538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113376069..113376342hg38UCSC Ensembl
chr9:116138349..116138622hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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