A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632709



Internal ID7019520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73431546..73432721hg38UCSC Ensembl
Innerchr13:73431569..73432698hg38UCSC Ensembl
Outerchr13:73431523..73432744hg38UCSC Ensembl
chr13:74005683..74006858hg19UCSC Ensembl
Innerchr13:74005706..74006835hg19UCSC Ensembl
Outerchr13:74005660..74006881hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14794265, essv14794267, essv14794266, essv14794264, essv14794272, essv14794273, essv14794269, essv14794271, essv14794270, essv14794268, essv14794263
SamplesNA21099, HG03687, NA12155, HG03910, HG03624, HG03902, HG03908, HG03787, HG02332, HG03743, HG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632709
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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