A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993784



Internal ID20560824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63330451..63340517hg38UCSC Ensembl
chr11:63097923..63107989hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3810067
hg1910067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461617
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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