A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671747



Internal ID9937852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185293614..185301326hg38UCSC Ensembl
Outerchr4:185293577..185301376hg38UCSC Ensembl
Innerchr4:186214768..186222480hg19UCSC Ensembl
Outerchr4:186214731..186222530hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5531115
SamplesHG01102
Known GenesSNX25
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671747
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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