A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086490



Internal ID21270669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:146900865..146907051hg38UCSC Ensembl
Innerchr6:147222001..147228187hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386187
hg196187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112901
Supporting Variants
Samplessample154
Known GenesSTXBP5-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086490
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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