A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697658



Internal ID15063369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11182176..11192774hg38UCSC Ensembl
InnerchrY:11183176..11191774hg38UCSC Ensembl
OuterchrY:11181176..11193774hg38UCSC Ensembl
chrY:13337852..13348450hg19UCSC Ensembl
InnerchrY:13338852..13347450hg19UCSC Ensembl
OuterchrY:13336852..13349450hg19UCSC Ensembl
chrY:11797852..11808450hg18UCSC Ensembl
InnerchrY:11798852..11807450hg18UCSC Ensembl
OuterchrY:11796852..11809450hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3810599
hg1910599
hg1810599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3368566
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697658
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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