A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633445



Internal ID7020254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105457162..105460959hg38UCSC Ensembl
Innerchr13:105457186..105460935hg38UCSC Ensembl
Outerchr13:105457138..105460983hg38UCSC Ensembl
chr13:106109511..106113308hg19UCSC Ensembl
Innerchr13:106109535..106113284hg19UCSC Ensembl
Outerchr13:106109487..106113332hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg383798
hg193798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14888856
SamplesNA21111
Known GenesDAOA-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633445
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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