A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700433



Internal ID21222273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83158722..83158722hg38UCSC Ensembl
chr9:85773637..85773637hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700433
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.90625


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