A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744095



Internal ID18718341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113700874..113701070hg38UCSC Ensembl
Outerchr9:113700834..113701103hg38UCSC Ensembl
Innerchr9:116463154..116463350hg19UCSC Ensembl
Outerchr9:116463114..116463383hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744095
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