A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13718764



Internal ID708421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24233855..24246661hg38UCSC Ensembl
chr10:24522784..24535590hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3812807
hg1912807
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622636
Supporting Variants
SamplesHG00332
Known GenesKIAA1217
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13718764
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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