A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632935



Internal ID7019746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83990163..84098873hg38UCSC Ensembl
Innerchr13:83990215..84098822hg38UCSC Ensembl
Outerchr13:83990112..84098925hg38UCSC Ensembl
chr13:84564298..84673008hg19UCSC Ensembl
Innerchr13:84564350..84672957hg19UCSC Ensembl
Outerchr13:84564247..84673060hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38108711
hg19108711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822399, essv14822395, essv14822400, essv14822398, essv14822396, essv14822397
SamplesHG02215, HG01354, HG00158, NA12889, HG01362, HG02351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632935
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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