A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29964



Internal ID12608158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81891311..81952513hg38UCSC Ensembl
Innerchr17:79849187..79910389hg19UCSC Ensembl
Innerchr17:77442483..77503679hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3861203
hg1961203
hg1861197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84203
SamplesHuRef
Known GenesALYREF, ANAPC11, MAFG, MAFG-AS1, MYADML2, NOTUM, NPB, PCYT2, PYCR1, SIRT7
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29964
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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