A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678564



Internal ID21200417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36295246..36295246hg38UCSC Ensembl
chr19:36786148..36786148hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385050
hg195050
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678564
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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