A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674239



Internal ID9940344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41114529..41119929hg38UCSC Ensembl
Outerchr3:41114495..41119964hg38UCSC Ensembl
Innerchr3:41156020..41161420hg19UCSC Ensembl
Outerchr3:41155986..41161455hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv858e199
Supporting Variantsessv6373450
SamplesNA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674239
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