A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141444



Internal ID340640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129058546..129072779hg38UCSC Ensembl
chr9:131820825..131835058hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814234
hg1914234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028050
Samples
Known GenesFAM73B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141444
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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