A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993783



Internal ID20560823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63326501..63328100hg38UCSC Ensembl
chr11:63093973..63095572hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462015
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00074


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