A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084151



Internal ID21268265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131166306..131183496hg38UCSC Ensembl
Innerchr7:130851065..130868255hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3817191
hg1917191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112551
Supporting Variants
Samplessample122
Known GenesMKLN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084151
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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