A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053323



Internal ID20620363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169710301..169711100hg38UCSC Ensembl
chr1:169679442..169680241hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320350
Supporting Variants
Samples
Known GenesSELL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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