A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7843389



Internal ID13622402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98443878..98443878hg38UCSC Ensembl
chr13:99096132..99096132hg19UCSC Ensembl
chr13:97894133..97894133hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3310565
Supporting Variants
SamplesNA12878
Known GenesFARP1
MethodSequencing
AnalysisCortex de-novo
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7843389
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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