A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685440



Internal ID21207301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8163059..8163059hg38UCSC Ensembl
chr17:8066377..8066377hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685440
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0714286


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