A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127375



Internal ID20694415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166333597..166334550hg38UCSC Ensembl
chr5:165760602..165761555hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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