A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6151482



Internal ID9128885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96300081..96305947hg38UCSC Ensembl
Outerchr13:96300044..96305997hg38UCSC Ensembl
Innerchr13:96952335..96958201hg19UCSC Ensembl
Outerchr13:96952298..96958251hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg385954
hg195954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659824
Supporting Variants
SamplesNA19449
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6151482
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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