A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8671928



Internal ID13387305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96658824..96658840hg38UCSC Ensembl
Innerchr10:96658822..96658840hg38UCSC Ensembl
Outerchr10:96658806..96658858hg38UCSC Ensembl
chr10:98418581..98418597hg19UCSC Ensembl
Innerchr10:98418579..98418597hg19UCSC Ensembl
Outerchr10:98418563..98418615hg19UCSC Ensembl
chr10:98408571..98408587hg18UCSC Ensembl
Innerchr10:98408587..98408569hg18UCSC Ensembl
Outerchr10:98408553..98408605hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3364401
Supporting Variants
SamplesNA12892
Known GenesPIK3AP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8671928
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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