A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7747123



Internal ID14518544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98137968..98137969hg38UCSC Ensembl
Innerchr10:98137923..98138014hg38UCSC Ensembl
Outerchr10:98137922..98138015hg38UCSC Ensembl
chr10:99897725..99897726hg19UCSC Ensembl
Innerchr10:99897680..99897771hg19UCSC Ensembl
Outerchr10:99897679..99897772hg19UCSC Ensembl
chr10:99887715..99887716hg18UCSC Ensembl
Innerchr10:99887761..99887670hg18UCSC Ensembl
Outerchr10:99887669..99887762hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303473
Supporting Variants
SamplesNA19114
Known GenesR3HCC1L
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7747123
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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