A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3343836



Internal ID15190820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10185895..10185895hg38UCSC Ensembl
InnerchrY:10185894..10185896hg38UCSC Ensembl
OuterchrY:10185835..10185945hg38UCSC Ensembl
chrY:10023504..10023504hg19UCSC Ensembl
InnerchrY:10023503..10023505hg19UCSC Ensembl
OuterchrY:10023444..10023554hg19UCSC Ensembl
chrY:10633504..10633504hg18UCSC Ensembl
InnerchrY:10633505..10633503hg18UCSC Ensembl
OuterchrY:10633444..10633554hg18UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8846988
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3343836
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