A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669901



Internal ID9589320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2835726..2838011hg38UCSC Ensembl
Outerchr3:2835689..2838061hg38UCSC Ensembl
Innerchr3:2877410..2879695hg19UCSC Ensembl
Outerchr3:2877373..2879745hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6150813
SamplesNA18606
Known GenesCNTN4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669901
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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