A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7764121



Internal ID13618817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98151043..98151044hg38UCSC Ensembl
Innerchr13:98151021..98151066hg38UCSC Ensembl
Outerchr13:98151020..98151067hg38UCSC Ensembl
chr13:98803297..98803298hg19UCSC Ensembl
Innerchr13:98803275..98803320hg19UCSC Ensembl
Outerchr13:98803274..98803321hg19UCSC Ensembl
chr13:97601298..97601299hg18UCSC Ensembl
Innerchr13:97601321..97601276hg18UCSC Ensembl
Outerchr13:97601275..97601322hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38293
hg19293
hg18293
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305227
Supporting Variants
SamplesNA12874
Known GenesFARP1
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7764121
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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