A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091914



Internal ID21276501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15156618..15181339hg38UCSC Ensembl
Innerchr11:15178164..15202885hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3824722
hg1924722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117626
Supporting Variants
Samplessample237
Known GenesINSC
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091914
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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