A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090849



Internal ID21274567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95504459..95510349hg38UCSC Ensembl
Innerchr9:98266741..98272631hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385891
hg195891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112342
Supporting Variants
Samplessample208
Known GenesPTCH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090849
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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