A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122620



Internal ID20689660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100826333..100943562hg38UCSC Ensembl
chr5:100162037..100279266hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38117230
hg19117230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396441
Supporting Variants
Samples
Known GenesST8SIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122620
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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