A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7753603



Internal ID14829793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100637959..100637960hg38UCSC Ensembl
Innerchr15:100637928..100637991hg38UCSC Ensembl
Outerchr15:100637927..100637992hg38UCSC Ensembl
chr15:101178164..101178165hg19UCSC Ensembl
Innerchr15:101178133..101178196hg19UCSC Ensembl
Outerchr15:101178132..101178197hg19UCSC Ensembl
chr15:98995687..98995688hg18UCSC Ensembl
Innerchr15:98995719..98995656hg18UCSC Ensembl
Outerchr15:98995655..98995720hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306872
Supporting Variants
SamplesNA19099
Known GenesASB7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7753603
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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