A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053449



Internal ID20620489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158699543..158740188hg38UCSC Ensembl
chr1:158669333..158709978hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3840646
hg1940646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322280
Supporting Variants
Samples
Known GenesOR6K2, OR6K3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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