A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671920



Internal ID9938025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38202933..38204080hg38UCSC Ensembl
Outerchr4:38202896..38204130hg38UCSC Ensembl
Innerchr4:38204554..38205701hg19UCSC Ensembl
Outerchr4:38204517..38205751hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6089595
SamplesNA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671920
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