A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5636799



Internal ID8614202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113431975..113440686hg38UCSC Ensembl
Outerchr13:113431938..113440736hg38UCSC Ensembl
Innerchr13:114086290..114095001hg19UCSC Ensembl
Outerchr13:114086253..114095051hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg388799
hg198799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677394
Supporting Variants
SamplesHG00699
Known GenesADPRHL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5636799
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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