A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006302



Internal ID7071395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42253551..42260400hg38UCSC Ensembl
Outerchr15:42545749..42552598hg19UCSC Ensembl
Outerchr15:40333041..40339890hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386850
hg196850
hg186850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564885
SamplesHuRef
Known GenesTMEM87A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006302
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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