A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996404



Internal ID20563445
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 StatusS
Merged Variantsnsv6459019
Supporting Variants
Samples
Known GenesCHORDC1, NAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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