A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697661



Internal ID13708521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11486176..11530174hg38UCSC Ensembl
InnerchrY:11487176..11529174hg38UCSC Ensembl
OuterchrY:11485176..11531174hg38UCSC Ensembl
chrY:13641852..13685850hg19UCSC Ensembl
InnerchrY:13642852..13684850hg19UCSC Ensembl
OuterchrY:13640852..13686850hg19UCSC Ensembl
chrY:12101852..12145850hg18UCSC Ensembl
InnerchrY:12102852..12144850hg18UCSC Ensembl
OuterchrY:12100852..12146850hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3843999
hg1943999
hg1843999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3336687
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697661
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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