A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950824



Internal ID16953011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144594617..144606615hg38UCSC Ensembl
Outerchr8:145820001..145832000hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3811999
hg1912000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999357
SamplesBILGI_BIOE
Known GenesARHGAP39
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950824
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer