A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992832



Internal ID20559872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73530269..73530995hg38UCSC Ensembl
chr11:73241314..73242040hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474391
Supporting Variants
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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