A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818273



Internal ID21263611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132421612..132421687hg38UCSC Ensembl
chr9:135296999..135297074hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698796
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818273
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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