A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8969330



Internal ID13459399
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 StatusS
Merged Variantsesv3386964
Supporting Variants
SamplesNA18504
Known GenesNTRK3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8969330
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer