A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13708103



Internal ID4945862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18089598..18118169hg38UCSC Ensembl
chr10:18378527..18407098hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3828572
hg1928572
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622500
Supporting Variants
SamplesNA12813
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13708103
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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