A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3324500



Internal ID15171478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27945887..27945898hg38UCSC Ensembl
Innerchr10:27945880..27945905hg38UCSC Ensembl
Outerchr10:27945869..27945916hg38UCSC Ensembl
chr10:28234816..28234827hg19UCSC Ensembl
Innerchr10:28234809..28234834hg19UCSC Ensembl
Outerchr10:28234798..28234845hg19UCSC Ensembl
chr10:28274822..28274833hg18UCSC Ensembl
Innerchr10:28274840..28274815hg18UCSC Ensembl
Outerchr10:28274804..28274851hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38123
hg19123
hg18123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8947757, essv8947759, essv8947749, essv8947754, essv8947755, essv8947750, essv8947753, essv8947748, essv8947745, essv8947751, essv8947752, essv8947746, essv8947756
SamplesNA18502, NA18508, NA18507, NA18504, NA18519, NA19099, NA18523, NA18909, NA19147, NA18501, NA19102, NA18511, NA18522
Known GenesARMC4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3324500
Frequency
Sample Size185
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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