A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8673252



Internal ID13737814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882878..82882883hg38UCSC Ensembl
chr15:83551630..83557686hg19UCSC Ensembl
Innerchr15:83551622..83557694hg19UCSC Ensembl
Outerchr15:83551616..83557700hg19UCSC Ensembl
chr15:81348684..81348690hg18UCSC Ensembl
Innerchr15:81348698..81348676hg18UCSC Ensembl
Outerchr15:81348670..81348704hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386032
hg196032
hg186032
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3375746
Supporting Variants
SamplesNA12892
Known GenesHOMER2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8673252
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