A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7836776



Internal ID14691164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30970443..30970444hg38UCSC Ensembl
Innerchr15:30970413..30970474hg38UCSC Ensembl
Outerchr15:30970412..30970475hg38UCSC Ensembl
chr15:31262646..31262647hg19UCSC Ensembl
Innerchr15:31262616..31262677hg19UCSC Ensembl
Outerchr15:31262615..31262678hg19UCSC Ensembl
chr15:29049938..29049939hg18UCSC Ensembl
Innerchr15:29049969..29049908hg18UCSC Ensembl
Outerchr15:29049907..29049970hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3309096
Supporting Variants
SamplesNA19239
Known GenesMTMR10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7836776
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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