A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143713



Internal ID342914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133946364..133952364hg38UCSC Ensembl
chr11:133816259..133822259hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051757
Samples
Known GenesIGSF9B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143713
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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