A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101652



Internal ID20668692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53855101..53865100hg38UCSC Ensembl
chr3:53889128..53899127hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359452
Supporting Variants
Samples
Known GenesIL17RB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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