A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3327507



Internal ID15174491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100637953..100637975hg38UCSC Ensembl
Innerchr15:100637959..100637967hg38UCSC Ensembl
Outerchr15:100637939..100637989hg38UCSC Ensembl
chr15:101178158..101178180hg19UCSC Ensembl
Innerchr15:101178164..101178172hg19UCSC Ensembl
Outerchr15:101178144..101178194hg19UCSC Ensembl
chr15:98995681..98995703hg18UCSC Ensembl
Innerchr15:98995695..98995687hg18UCSC Ensembl
Outerchr15:98995667..98995717hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8970021, essv8970018, essv8970017, essv8970019, essv8970020
SamplesNA18545, NA18526, NA19099, NA19257, NA19147
Known GenesASB7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3327507
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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