A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3552302



Internal ID18406692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35238861..35243299hg38UCSC Ensembl
Outerchr15:35237800..35243799hg38UCSC Ensembl
Innerchr15:35531062..35535500hg19UCSC Ensembl
Outerchr15:35530001..35536000hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9751049
Samples
Known GenesANP32AP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3552302
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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