A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090247



Internal ID21286873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75057397..75086715hg38UCSC Ensembl
Innerchr11:74768442..74797760hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3829319
hg1929319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111175
Supporting Variants
Samplessample395
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090247
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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