A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051113



Internal ID20618153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108559801..108560400hg38UCSC Ensembl
chr1:109102423..109103022hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323797
Supporting Variants
Samples
Known GenesFAM102B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08996


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