A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677579



Internal ID9943684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13291067..13297868hg38UCSC Ensembl
chr3:13332567..13339368hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386802
hg196802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5816213, essv6262569, essv5442182
SamplesHG00654, HG00683, HG00705
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677579
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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