A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697657



Internal ID13708588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11181676..11199274hg38UCSC Ensembl
InnerchrY:11182676..11198274hg38UCSC Ensembl
OuterchrY:11180676..11200274hg38UCSC Ensembl
chrY:13337352..13354950hg19UCSC Ensembl
InnerchrY:13338352..13353950hg19UCSC Ensembl
OuterchrY:13336352..13355950hg19UCSC Ensembl
chrY:11797352..11814950hg18UCSC Ensembl
InnerchrY:11798352..11813950hg18UCSC Ensembl
OuterchrY:11796352..11815950hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3817599
hg1917599
hg1817599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3395210
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697657
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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