A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6299006



Internal ID9276409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87893066..87893965hg38UCSC Ensembl
chr10:89652823..89653722hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678342
Supporting Variants
SamplesHG00237
Known GenesPTEN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6299006
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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