A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085776



Internal ID21266618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91302266..91306394hg38UCSC Ensembl
Innerchr8:92314494..92318622hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg384129
hg194129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115225
Supporting Variants
Samplessample10
Known GenesSLC26A7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085776
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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