A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7737463



Internal ID14552727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86524768..86524769hg38UCSC Ensembl
Outerchr10:86524618..86524919hg38UCSC Ensembl
Innerchr10:88284525..88284526hg19UCSC Ensembl
Outerchr10:88284375..88284676hg19UCSC Ensembl
Innerchr10:88274506..88274505hg18UCSC Ensembl
Outerchr10:88274355..88274656hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38302
hg19302
hg18302
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302874
Supporting Variants
SamplesNA19137
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7737463
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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