A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751570



Internal ID18725816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89296220..89296360hg38UCSC Ensembl
Outerchr15:89296216..89296363hg38UCSC Ensembl
Innerchr15:89839451..89839591hg19UCSC Ensembl
Outerchr15:89839447..89839594hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552823
Supporting Variants
Samples
Known GenesFANCI
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751570
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