A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758281



Internal ID18732527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:13606121..13619492hg38UCSC Ensembl
OuterchrY:13606089..13619620hg38UCSC Ensembl
InnerchrY:15718001..15731372hg19UCSC Ensembl
OuterchrY:15717969..15731500hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3813532
hg1913532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758281
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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