A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985537



Internal ID20552577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100991602..100992433hg38UCSC Ensembl
chr11:100862333..100863164hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472924
Supporting Variants
Samples
Known GenesTMEM133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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