A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818228



Internal ID21263566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109562387..109562387hg38UCSC Ensembl
chr9:112324667..112324667hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706157, nssv13701449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818228
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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