A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307702



Internal ID14807964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88086489..88086490hg38UCSC Ensembl
Innerchr15:88086456..88086523hg38UCSC Ensembl
Outerchr15:88086455..88086524hg38UCSC Ensembl
chr15:88629720..88629721hg19UCSC Ensembl
Innerchr15:88629687..88629754hg19UCSC Ensembl
Outerchr15:88629686..88629755hg19UCSC Ensembl
chr15:86430724..86430725hg18UCSC Ensembl
Innerchr15:86430758..86430691hg18UCSC Ensembl
Outerchr15:86430690..86430759hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38263
hg19263
hg18263
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7762241, essv7746825, essv7744109, essv7761464, essv7755188, essv7740590, essv7754090, essv7760320, essv7745346, essv7741104
SamplesNA18523, NA18517, NA18489, NA19147, NA18510, NA18504, NA19138, NA19116, NA18499, NA18853
Known GenesNTRK3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307702
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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