A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668778



Internal ID9934883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33705174..33712309hg38UCSC Ensembl
Outerchr4:33705017..33712462hg38UCSC Ensembl
Innerchr4:33706796..33713931hg19UCSC Ensembl
Outerchr4:33706639..33714084hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg387446
hg197446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5508349
SamplesNA07051
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668778
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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