A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697666



Internal ID13708620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11677946..11749544hg38UCSC Ensembl
InnerchrY:11678946..11748544hg38UCSC Ensembl
OuterchrY:11677873..11750544hg38UCSC Ensembl
chrY:13798652..13870250hg19UCSC Ensembl
InnerchrY:13799652..13869250hg19UCSC Ensembl
OuterchrY:13798579..13871250hg19UCSC Ensembl
chrY:12308652..12380250hg18UCSC Ensembl
InnerchrY:12309652..12379250hg18UCSC Ensembl
OuterchrY:12307652..12381250hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3871599
hg1971599
hg1871599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3340854
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697666
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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