A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550918



Internal ID18405308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95240947..95241780hg38UCSC Ensembl
Outerchr13:95240895..95241800hg38UCSC Ensembl
Innerchr13:95893201..95894034hg19UCSC Ensembl
Outerchr13:95893149..95894054hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749665
Samples
Known GenesABCC4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550918
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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