A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8691353



Internal ID15105709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79145164..79146662hg38UCSC Ensembl
Innerchr18:79145662..79146164hg38UCSC Ensembl
Outerchr18:79144164..79147662hg38UCSC Ensembl
chr18:76905164..76906662hg19UCSC Ensembl
Innerchr18:76905662..76906164hg19UCSC Ensembl
Outerchr18:76904164..76907662hg19UCSC Ensembl
chr18:75006152..75007650hg18UCSC Ensembl
Innerchr18:75007152..75006650hg18UCSC Ensembl
Outerchr18:75005152..75008650hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3384311
Supporting Variants
SamplesNA19240
Known GenesATP9B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8691353
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