A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678298



Internal ID21200159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219411128..219411246hg38UCSC Ensembl
chr1:219584470..219584588hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678298
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09375


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