A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988217



Internal ID20555257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133900034..133900341hg38UCSC Ensembl
chr11:133769929..133770236hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456064
Supporting Variants
Samples
Known GenesMIR4697HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00204


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