A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678454



Internal ID9597873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159462786..159465654hg38UCSC Ensembl
chr3:159180575..159183443hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382869
hg192869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6172989
SamplesNA10847
Known GenesIQCJ-SCHIP1, SCHIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678454
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