A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666502



Internal ID9932607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120078646..120079017hg38UCSC Ensembl
Outerchr3:120078609..120079067hg38UCSC Ensembl
Innerchr3:119797493..119797864hg19UCSC Ensembl
Outerchr3:119797456..119797914hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6116155
SamplesHG00533
Known GenesGSK3B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666502
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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