A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087979



Internal ID21279015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69841418..69846171hg38UCSC Ensembl
Innerchr9:72456334..72461087hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg384754
hg194754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115799
Supporting Variants
Samplessample276
Known GenesC9orf135
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087979
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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