A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758296



Internal ID18732542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:20792115..20829457hg38UCSC Ensembl
OuterchrY:20791945..20829614hg38UCSC Ensembl
InnerchrY:22954001..22991343hg19UCSC Ensembl
OuterchrY:22953831..22991500hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3837670
hg1937670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758296
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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