A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135160



Internal ID20702200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83529550..83530131hg38UCSC Ensembl
chr5:82825369..82825950hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396598
Supporting Variants
Samples
Known GenesVCAN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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