A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086667



Internal ID21282355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76048581..76053543hg38UCSC Ensembl
Innerchr7:75677899..75682861hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384963
hg194963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114112
Supporting Variants
Samplessample325
Known GenesMDH2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086667
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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