A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659732



Internal ID9579151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161289101..161290233hg38UCSC Ensembl
chr5:160716108..160717240hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5766431
SamplesNA18867
Known GenesGABRB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659732
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