A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996067



Internal ID20563107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99091701..99099300hg38UCSC Ensembl
chr11:98962431..98970030hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464795
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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