A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467597



Internal ID21125150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134223601..134226700hg38UCSC Ensembl
chr11:134093495..134096594hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188393
Samples
Known GenesNCAPD3, VPS26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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