A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14881019



Internal ID4882836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103031398..103049232hg38UCSC Ensembl
chr13:103683748..103701582hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3817835
hg1917835
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633387
Supporting Variants
SamplesHG01710
Known GenesSLC10A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14881019
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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