A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661772



Internal ID9927877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124203854..124210616hg38UCSC Ensembl
chr5:123539547..123546309hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg386763
hg196763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6089506, essv5548591
SamplesNA19904, NA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661772
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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