A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084237



Internal ID21269334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11830292..11833822hg38UCSC Ensembl
Innerchr7:11869918..11873448hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg383531
hg193531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114362
Supporting Variants
Samplessample138
Known GenesTHSD7A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084237
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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