A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352378



Internal ID22578047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109071684..109072275hg38UCSC Ensembl
chr1:109614306..109614897hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880589
Supporting Variants
Samples
Known GenesTAF13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352378
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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