A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089752



Internal ID21271198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85287656..85292443hg38UCSC Ensembl
Innerchr9:87902571..87907358hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384788
hg194788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116577
Supporting Variants
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089752
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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