A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633057



Internal ID7019867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88009927..88030992hg38UCSC Ensembl
Innerchr13:88009957..88030962hg38UCSC Ensembl
Outerchr13:88009897..88031022hg38UCSC Ensembl
chr13:88662182..88683247hg19UCSC Ensembl
Innerchr13:88662212..88683217hg19UCSC Ensembl
Outerchr13:88662152..88683277hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3821066
hg1921066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14834869
SamplesHG00264
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633057
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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