A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993781



Internal ID20560821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63312281..63313069hg38UCSC Ensembl
chr11:63079753..63080541hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465616
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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