A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865004



Internal ID13317694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24525825..24525832hg38UCSC Ensembl
Innerchr10:24525809..24525848hg38UCSC Ensembl
Outerchr10:24525802..24525855hg38UCSC Ensembl
chr10:24814754..24814761hg19UCSC Ensembl
Innerchr10:24814738..24814777hg19UCSC Ensembl
Outerchr10:24814731..24814784hg19UCSC Ensembl
chr10:24854760..24854767hg18UCSC Ensembl
Innerchr10:24854783..24854744hg18UCSC Ensembl
Outerchr10:24854737..24854790hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3399906
Supporting Variants
SamplesNA12005
Known GenesKIAA1217
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865004
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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