A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633278



Internal ID6673400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96685999..96687827hg38UCSC Ensembl
Innerchr13:96685999..96687827hg38UCSC Ensembl
Outerchr13:96685947..96687866hg38UCSC Ensembl
chr13:97338253..97340081hg19UCSC Ensembl
Innerchr13:97338253..97340081hg19UCSC Ensembl
Outerchr13:97338201..97340120hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381829
hg191829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869337
SamplesHG02554
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633278
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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