A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141722



Internal ID340919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66775887..67200246hg38UCSC Ensembl
chr9:40492595..40916995hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38424360
hg19424401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024164
Samples
Known GenesFAM74A3, SPATA31A3, ZNF658
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141722
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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