A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662927



Internal ID9929032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102005629..102017277hg38UCSC Ensembl
chr13:102657979..102669627hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3811649
hg1911649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6128842
SamplesNA19000
Known GenesFGF14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662927
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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