A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683545



Internal ID21205403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226114946..226114995hg38UCSC Ensembl
chr1:226302647..226302696hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683545
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.133333


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