A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985658



Internal ID20552698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104891586..104990021hg38UCSC Ensembl
chr11:104762313..104860748hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3898436
hg1998436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455764
Supporting Variants
Samples
Known GenesCASP12, CASP4, LOC643733
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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