A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3365060



Internal ID14865320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32821087..32821106hg38UCSC Ensembl
Innerchr15:32821083..32821110hg38UCSC Ensembl
Outerchr15:32821064..32821129hg38UCSC Ensembl
chr15:33113288..33113307hg19UCSC Ensembl
Innerchr15:33113284..33113311hg19UCSC Ensembl
Outerchr15:33113265..33113330hg19UCSC Ensembl
chr15:30900580..30900599hg18UCSC Ensembl
Innerchr15:30900603..30900576hg18UCSC Ensembl
Outerchr15:30900557..30900622hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9667936, essv9667958, essv9667947
SamplesNA12873, NA12814, NA12045
Known GenesFMN1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3365060
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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