A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662736



Internal ID9928841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2434861..2444562hg38UCSC Ensembl
Outerchr4:2434824..2444612hg38UCSC Ensembl
Innerchr4:2436588..2446289hg19UCSC Ensembl
Outerchr4:2436551..2446339hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg389789
hg199789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5620770
SamplesHG00343
Known GenesLOC402160
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662736
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer