A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473096



Internal ID21130649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125702356..125790716hg38UCSC Ensembl
chr11:125572251..125660611hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3888361
hg1988361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195469
Samples
Known GenesPATE1, PATE2, PATE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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