A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559454



Internal ID18760530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24832216..24835011hg38UCSC Ensembl
Outerchr1:24832129..24835291hg38UCSC Ensembl
Innerchr1:25158707..25161502hg19UCSC Ensembl
Outerchr1:25158620..25161782hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758201
Samples
Known GenesCLIC4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559454
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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