A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3386964



Internal ID14887246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88086485..88086509hg38UCSC Ensembl
Innerchr15:88086491..88086501hg38UCSC Ensembl
Outerchr15:88086467..88086527hg38UCSC Ensembl
chr15:88629716..88629740hg19UCSC Ensembl
Innerchr15:88629722..88629732hg19UCSC Ensembl
Outerchr15:88629698..88629758hg19UCSC Ensembl
chr15:86430720..86430744hg18UCSC Ensembl
Innerchr15:86430736..86430726hg18UCSC Ensembl
Outerchr15:86430702..86430762hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38263
hg19263
hg18263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8969331, essv8969330, essv8969333, essv8969332, essv8969334, essv8969326, essv8969327, essv8969335, essv8969328, essv8969329
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)esv3386964
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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