A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475099



Internal ID21132652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33273227..33459782hg38UCSC Ensembl
chr11:33294773..33481328hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38186556
hg19186556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1022n223
Supporting Variantsnssv18187255
Samples
Known GenesHIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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