A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992008



Internal ID20559048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59209190..59214978hg38UCSC Ensembl
chr11:58976663..58982451hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385789
hg195789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473550
Supporting Variants
Samples
Known GenesMPEG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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