A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657433



Internal ID9923538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186777032..186778873hg38UCSC Ensembl
Outerchr3:186776995..186778923hg38UCSC Ensembl
Innerchr3:186494821..186496662hg19UCSC Ensembl
Outerchr3:186494784..186496712hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381929
hg191929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6587298
SamplesNA19717
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657433
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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