A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5764399



Internal ID9106632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57551985..57557048hg38UCSC Ensembl
Outerchr2:57551828..57557201hg38UCSC Ensembl
Innerchr2:57779120..57784183hg19UCSC Ensembl
Outerchr2:57778963..57784336hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385374
hg195374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662456
Supporting Variants
SamplesHG01101
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5764399
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