A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663898



Internal ID9583317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2574157..2575452hg38UCSC Ensembl
chr3:2615841..2617136hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6112033, essv6378201, essv6424779, essv5419718
SamplesNA19819, NA19451, NA19471, NA19429
Known GenesCNTN4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663898
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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