A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659856



Internal ID9925961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19478740..19506998hg38UCSC Ensembl
Outerchr4:19478703..19507048hg38UCSC Ensembl
Innerchr4:19480363..19508621hg19UCSC Ensembl
Outerchr4:19480326..19508671hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3828346
hg1928346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5872706
SamplesHG00654
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659856
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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