A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141912



Internal ID341111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66591387..66713846hg38UCSC Ensembl
chr9:41808145..41930502hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38122460
hg19122358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141912
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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