A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087939



Internal ID21278058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130960328..130979833hg38UCSC Ensembl
Innerchr9:133835715..133855220hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3819506
hg1919506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112289
Supporting Variants
Samplessample263
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087939
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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