A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141586



Internal ID340783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67601500..67617400hg38UCSC Ensembl
chr9:44748037..46275929hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3815901
hg191527893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024212
Samples
Known GenesFAM27A, FAM27C, FAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141586
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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