A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134740



Internal ID20701780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87668585..87669189hg38UCSC Ensembl
chr5:86964402..86965006hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395738
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0011


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