A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663932



Internal ID9930037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88194497..88199957hg38UCSC Ensembl
chr4:89115649..89121109hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg385461
hg195461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5495327
SamplesNA19383
Known GenesABCG2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663932
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