A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310444



Internal ID15157395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36780807..36780807hg38UCSC Ensembl
Outerchr3:36780807..36780807hg38UCSC Ensembl
Innerchr3:36822298..36822298hg19UCSC Ensembl
Outerchr3:36822298..36822298hg19UCSC Ensembl
Innerchr3:36797302..36797302hg18UCSC Ensembl
Outerchr3:36797302..36797302hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38578
hg19578
hg18578
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843577
SamplesNA19240
Known Genes
MethodSequencing
AnalysisNovelSeq
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310444
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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