A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660605



Internal ID9580024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108912003..108913848hg38UCSC Ensembl
Outerchr3:108911846..108914001hg38UCSC Ensembl
Innerchr3:108630850..108632695hg19UCSC Ensembl
Outerchr3:108630693..108632848hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382156
hg192156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6252557
SamplesNA19921
Known GenesGUCA1C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660605
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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