A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4637e59



Internal ID22765857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11677873..11749544hg38UCSC Ensembl
chrY:13798579..13870250hg19UCSC Ensembl
chrY:12308552..12380250hg18UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3871672
hg1971672
hg1871699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3340854, esv3345384
SamplesNA12891, NA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4637e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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