A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697674



Internal ID13708657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56673215..56771507hg38UCSC Ensembl
InnerchrY:56674209..56770507hg38UCSC Ensembl
OuterchrY:56673215..56771509hg38UCSC Ensembl
chrY:58819364..58917656hg19UCSC Ensembl
InnerchrY:58820364..58916662hg19UCSC Ensembl
OuterchrY:58819362..58917656hg19UCSC Ensembl
chrY:57228752..57327050hg18UCSC Ensembl
InnerchrY:57229752..57326050hg18UCSC Ensembl
OuterchrY:57227752..57328050hg18UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3898293
hg1998293
hg1898299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3440347
Supporting Variants
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697674
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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