A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9745744



Internal ID18719990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125313886..125316157hg38UCSC Ensembl
Outerchr10:125313828..125316421hg38UCSC Ensembl
Innerchr10:127002455..127004726hg19UCSC Ensembl
Outerchr10:127002397..127004990hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382594
hg192594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3546997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9745744
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