A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3382544



Internal ID15229515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9333543..9334041hg38UCSC Ensembl
InnerchrY:9333542..9334042hg38UCSC Ensembl
OuterchrY:9332543..9335041hg38UCSC Ensembl
chrY:9171152..9171650hg19UCSC Ensembl
InnerchrY:9171151..9171651hg19UCSC Ensembl
OuterchrY:9170152..9172650hg19UCSC Ensembl
chrY:9231152..9231650hg18UCSC Ensembl
InnerchrY:9231651..9231151hg18UCSC Ensembl
OuterchrY:9230152..9232650hg18UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697677
SamplesNA19239
Known GenesTTTY20
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3382544
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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