A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087899



Internal ID21276926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95503356..95512670hg38UCSC Ensembl
Innerchr9:98265638..98274952hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg389315
hg199315
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117730
Supporting Variants
Samplessample243
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087899
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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