A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402032



Internal ID22459902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10451734..10452295hg38UCSC Ensembl
chr20:10432382..10432943hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927717
Supporting Variants
Samples
Known GenesSLX4IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402032
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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