A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758302



Internal ID18732548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:56839646..56843613hg38UCSC Ensembl
OuterchrY:56838875..56844350hg38UCSC Ensembl
InnerchrY:58985793..58989760hg19UCSC Ensembl
OuterchrY:58985022..58990497hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg385476
hg195476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758302
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer