A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3448938



Internal ID15295887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39484352..39484371hg38UCSC Ensembl
Innerchr15:39484348..39484375hg38UCSC Ensembl
Outerchr15:39484329..39484394hg38UCSC Ensembl
chr15:39776553..39776572hg19UCSC Ensembl
Innerchr15:39776549..39776576hg19UCSC Ensembl
Outerchr15:39776530..39776595hg19UCSC Ensembl
chr15:37563845..37563864hg18UCSC Ensembl
Innerchr15:37563868..37563841hg18UCSC Ensembl
Outerchr15:37563822..37563887hg18UCSC Ensembl
Cytoband15q14
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 Variantsessv9668258, essv9668247
SamplesNA07346, NA12812
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3448938
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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