A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141484



Internal ID340681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138227536..138235536hg38UCSC Ensembl
chr9:141117986..141125986hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029804
Samples
Known GenesFAM157B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141484
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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