A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17498158



Internal ID22556093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75250293..75264983hg38UCSC Ensembl
chr5:74546118..74560808hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3814691
hg1914691
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17498158
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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