A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633132



Internal ID7019942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90654668..90667879hg38UCSC Ensembl
Innerchr13:90654668..90667879hg38UCSC Ensembl
Outerchr13:90654168..90668379hg38UCSC Ensembl
chr13:91306922..91320133hg19UCSC Ensembl
Innerchr13:91306922..91320133hg19UCSC Ensembl
Outerchr13:91306422..91320633hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3813212
hg1913212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv361e214
Supporting Variantsessv14848200, essv14848197, essv14848199, essv14848201, essv14848198, essv14848196
SamplesNA19457, HG03058, HG03061, HG03563, HG01894, HG03084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633132
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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