A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660877



Internal ID9926982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238965072..238965222hg38UCSC Ensembl
chr2:239886768..239886918hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6326249, essv6029276, essv6204120, essv5730396, essv6317646, essv6107023, essv6358931
SamplesNA18545, NA18526, NA18566, HG00651, HG00250, NA18612, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660877
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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