A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475431



Internal ID21132984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129143072..129145383hg38UCSC Ensembl
chr11:129012967..129015278hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382312
hg192312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185579
Samples
Known GenesARHGAP32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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