A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633592



Internal ID7020401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112905441..112907968hg38UCSC Ensembl
Innerchr13:112905450..112907960hg38UCSC Ensembl
Outerchr13:112905433..112907977hg38UCSC Ensembl
chr13:113559755..113562282hg19UCSC Ensembl
Innerchr13:113559764..113562274hg19UCSC Ensembl
Outerchr13:113559747..113562291hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382528
hg192528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14904185, essv14904184
SamplesHG01840, HG02390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633592
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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