A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668691



Internal ID9588110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81627337..81643581hg38UCSC Ensembl
Outerchr3:81627300..81643631hg38UCSC Ensembl
Innerchr3:81676488..81692732hg19UCSC Ensembl
Outerchr3:81676451..81692782hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3816332
hg1916332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5795754
SamplesHG00595
Known GenesGBE1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668691
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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