A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996356



Internal ID20563397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89416014..89461520hg38UCSC Ensembl
chr11:89149182..89194688hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3845507
hg1945507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457095
Supporting Variants
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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