A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6287043



Internal ID9264446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96267537..96273699hg38UCSC Ensembl
chr13:96919791..96925953hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg386163
hg196163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662908
Supporting Variants
SamplesNA18523
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6287043
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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