A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3400844



Internal ID15247807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79376690..79379288hg38UCSC Ensembl
Innerchr10:79377690..79378288hg38UCSC Ensembl
Outerchr10:79375690..79380288hg38UCSC Ensembl
chr10:81136446..81139044hg19UCSC Ensembl
Innerchr10:81137446..81138044hg19UCSC Ensembl
Outerchr10:81135446..81140044hg19UCSC Ensembl
chr10:80806452..80809050hg18UCSC Ensembl
Innerchr10:80807452..80808050hg18UCSC Ensembl
Outerchr10:80805452..80810050hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv464e59
Supporting Variantsessv8688140
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3400844
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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