A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705275



Internal ID21227079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115347136..115347136hg38UCSC Ensembl
chr19:34570031..34570031hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705275
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.875


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