A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088045



Internal ID21281032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95504459..95514540hg38UCSC Ensembl
Innerchr9:98266741..98276822hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3810082
hg1910082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113724
Supporting Variants
Samplessample306
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088045
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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