A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632055



Internal ID7018865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49809104..49818105hg38UCSC Ensembl
Innerchr13:49809140..49818069hg38UCSC Ensembl
Outerchr13:49809068..49818141hg38UCSC Ensembl
chr13:50383240..50392241hg19UCSC Ensembl
Innerchr13:50383276..50392205hg19UCSC Ensembl
Outerchr13:50383204..50392277hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg389002
hg199002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14725716
SamplesHG02445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632055
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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