A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141806



Internal ID341004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128052552..128060552hg38UCSC Ensembl
chr9:130814831..130822831hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141806
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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