A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545273



Internal ID18746349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107670623..107670881hg38UCSC Ensembl
Outerchr9:107670555..107670968hg38UCSC Ensembl
Innerchr9:110432904..110433162hg19UCSC Ensembl
Outerchr9:110432836..110433249hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744020
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545273
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