A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668502



Internal ID9934607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157701943..157704119hg38UCSC Ensembl
Outerchr3:157701756..157704303hg38UCSC Ensembl
Innerchr3:157419732..157421908hg19UCSC Ensembl
Outerchr3:157419545..157422092hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6429816, essv5785079
SamplesHG00654, NA18576
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668502
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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