A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819108



Internal ID21264446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132526544..132529524hg38UCSC Ensembl
chr9:135401931..135404911hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701207
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819108
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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