A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624806



Internal ID7011656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124267193..124270605hg38UCSC Ensembl
chr10:125955762..125959174hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383413
hg193413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963171, essv13963172
SamplesHG01049, HG00513
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624806
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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