A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094599



Internal ID21270315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44139389..44145560hg38UCSC Ensembl
Innerchr13:44713525..44719696hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg386172
hg196172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116026
Supporting Variants
Samplessample149
Known GenesSMIM2, SMIM2-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094599
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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