A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666464



Internal ID9932569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35821135..35840227hg38UCSC Ensembl
Outerchr4:35821098..35840277hg38UCSC Ensembl
Innerchr4:35822757..35841849hg19UCSC Ensembl
Outerchr4:35822720..35841899hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3819180
hg1919180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5930748
SamplesHG00133
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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