A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668678



Internal ID9588097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11701172..11701909hg38UCSC Ensembl
Outerchr2:11701135..11701959hg38UCSC Ensembl
Innerchr2:11841298..11842035hg19UCSC Ensembl
Outerchr2:11841261..11842085hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6332030
SamplesNA20753
Known GenesLPIN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668678
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