A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688895



Internal ID13696206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21153613..21155311hg38UCSC Ensembl
Innerchr13:21154311..21154613hg38UCSC Ensembl
Outerchr13:21152613..21156311hg38UCSC Ensembl
chr13:21727752..21729450hg19UCSC Ensembl
Innerchr13:21728450..21728752hg19UCSC Ensembl
Outerchr13:21726752..21730450hg19UCSC Ensembl
chr13:20625752..20627450hg18UCSC Ensembl
Innerchr13:20626752..20626450hg18UCSC Ensembl
Outerchr13:20624752..20628450hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3336873
Supporting Variants
SamplesNA12891
Known GenesSKA3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688895
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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