A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995227



Internal ID20562267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93396385..93397047hg38UCSC Ensembl
chr11:93129551..93130213hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459946
Supporting Variants
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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