A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302624



Internal ID14802886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86524708..86524812hg38UCSC Ensembl
Innerchr10:86524760..86524760hg38UCSC Ensembl
Outerchr10:86524608..86524912hg38UCSC Ensembl
chr10:88284465..88284569hg19UCSC Ensembl
Innerchr10:88284517..88284517hg19UCSC Ensembl
Outerchr10:88284365..88284669hg19UCSC Ensembl
chr10:88274445..88274549hg18UCSC Ensembl
Innerchr10:88274497..88274497hg18UCSC Ensembl
Outerchr10:88274345..88274649hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38105
hg19105
hg18105
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv469e59
Supporting Variantsessv7731178, essv7731420, essv7731067, essv7731632, essv7730861
SamplesNA12891, NA19238, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302624
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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