A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415408



Internal ID15262367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11286076..11334474hg38UCSC Ensembl
InnerchrY:11287076..11333474hg38UCSC Ensembl
OuterchrY:11285076..11335474hg38UCSC Ensembl
chrY:13441752..13490150hg19UCSC Ensembl
InnerchrY:13442752..13489150hg19UCSC Ensembl
OuterchrY:13440752..13491150hg19UCSC Ensembl
chrY:11901752..11950150hg18UCSC Ensembl
InnerchrY:11902752..11949150hg18UCSC Ensembl
OuterchrY:11900752..11951150hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3848399
hg1948399
hg1848399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4635e59
Supporting Variantsessv8697659
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415408
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