A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661783



Internal ID9927888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241078124..241079152hg38UCSC Ensembl
chr2:242017539..242018567hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv772e199
Supporting Variantsessv5818358, essv5568296, essv5832994, essv6294726
SamplesNA19443, NA19469, NA19331, NA19470
Known GenesSNED1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661783
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