A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459019



Internal ID21116572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90190987..90232983hg38UCSC Ensembl
chr11:89924155..89966151hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3841997
hg1941997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996404
Samples
Known GenesCHORDC1, NAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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