A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467899



Internal ID21125452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74300301..74405700hg38UCSC Ensembl
chr11:74011346..74116745hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38105400
hg19105400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193838
Samples
Known GenesP4HA3, PGM2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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