A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985476



Internal ID20552516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102434001..102436700hg38UCSC Ensembl
chr11:102304732..102307431hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462119
Supporting Variants
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01074


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