A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13718762



Internal ID708391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24232587..24260424hg38UCSC Ensembl
chr10:24521516..24549353hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3827838
hg1927838
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622635
Supporting Variants
SamplesHG00332
Known GenesKIAA1217
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13718762
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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