A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996450



Internal ID20563490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93151305..93151807hg38UCSC Ensembl
chr11:92884471..92884973hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457869
Supporting Variants
Samples
Known GenesSLC36A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00068


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