A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6182011



Internal ID9805756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98244293..98246266hg38UCSC Ensembl
chr13:98896547..98898520hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657451
Supporting Variants
SamplesNA19904
Known GenesFARP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6182011
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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