A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631942



Internal ID7018752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44833784..44854465hg38UCSC Ensembl
chr13:45407920..45428601hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3820682
hg1920682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv331e214
Supporting Variantsessv14710601, essv14710600
SamplesNA18565, HG00631
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631942
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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