A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136160



Internal ID20703200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93603901..93604600hg38UCSC Ensembl
chr5:92939607..92940306hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415166
Supporting Variants
Samples
Known GenesMIR548AO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00404


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