A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29990



Internal ID12954870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135328379..135372394hg38UCSC Ensembl
Innerchr7:135013131..135057146hg19UCSC Ensembl
Innerchr7:134663671..134707686hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3844016
hg1944016
hg1844016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84229
SamplesHuRef
Known GenesCNOT4
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29990
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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