A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992828



Internal ID20559868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73448333..73458846hg38UCSC Ensembl
chr11:73159378..73169891hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3810514
hg1910514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463318
Supporting Variants
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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