A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743925



Internal ID18718171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97998798..97999054hg38UCSC Ensembl
Outerchr9:97998741..97999124hg38UCSC Ensembl
Innerchr9:100761080..100761336hg19UCSC Ensembl
Outerchr9:100761023..100761406hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545178
Supporting Variants
Samples
Known GenesANP32B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743925
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