A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141842



Internal ID341041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137201536..137243536hg38UCSC Ensembl
chr9:140095988..140137988hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3842001
hg1942001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029643
Samples
Known GenesC9orf169, NDOR1, RNF208, RNF224, SLC34A3, TMEM203, TUBB4B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141842
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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