A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992781



Internal ID20559821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72413170..72416529hg38UCSC Ensembl
chr11:72124214..72127573hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462511
Supporting Variants
Samples
Known GenesCLPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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