A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6516902



Internal ID9494306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69175268..69175322hg38UCSC Ensembl
chr5:68471095..68471149hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671857
Supporting Variants
SamplesNA12005
Known GenesCCNB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6516902
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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