A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091783



Internal ID21272692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14435529..14443085hg38UCSC Ensembl
Innerchr11:14457075..14464631hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg387557
hg197557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116099
Supporting Variants
Samplessample180
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091783
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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