A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29997



Internal ID12608191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25289645..25321967hg38UCSC Ensembl
Innerchr1:25616136..25648458hg19UCSC Ensembl
Innerchr1:25488723..25521045hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3832323
hg1932323
hg1832323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84236
SamplesHuRef
Known GenesRHD
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29997
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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