A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631556



Internal ID6671682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24426828..24487208hg38UCSC Ensembl
Innerchr13:24426878..24487158hg38UCSC Ensembl
Outerchr13:24426778..24487258hg38UCSC Ensembl
chr13:25000966..25061346hg19UCSC Ensembl
Innerchr13:25001016..25061296hg19UCSC Ensembl
Outerchr13:25000916..25061396hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3860381
hg1960381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14671210
SamplesHG03693
Known GenesPARP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631556
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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