A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493133



Internal ID22551061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114139681..114174847hg38UCSC Ensembl
chr5:113475378..113510544hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3835167
hg1935167
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493133
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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