A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000872



Internal ID7066001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24869599..24875610hg38UCSC Ensembl
Outerchr15:25114746..25120757hg19UCSC Ensembl
Outerchr15:22665839..22671850hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386012
hg196012
hg186012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564185
SamplesHuRef
Known GenesSNRPN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000872
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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