A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089699



Internal ID21269578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15611325..15623353hg38UCSC Ensembl
Innerchr9:15611323..15623351hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3812029
hg1912029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113143
Supporting Variants
Samplessample140
Known GenesCCDC171
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089699
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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