A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5853315



Internal ID9795663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:33558679..33565085hg38UCSC Ensembl
Outerchr13:33558308..33565455hg38UCSC Ensembl
Innerchr13:34132816..34139222hg19UCSC Ensembl
Outerchr13:34132445..34139592hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg387148
hg197148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670631
Supporting Variants
SamplesNA19818
Known GenesSTARD13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5853315
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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