A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817334



Internal ID21262672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132519455..132519455hg38UCSC Ensembl
chr9:135394842..135394842hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704565
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817334
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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