A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751395



Internal ID18725641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71182162..71185212hg38UCSC Ensembl
Outerchr15:71181289..71185779hg38UCSC Ensembl
Innerchr15:71474501..71477551hg19UCSC Ensembl
Outerchr15:71473628..71478118hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384491
hg194491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552648
Supporting Variants
Samples
Known GenesTHSD4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751395
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