A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149497



Internal ID19203226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32740275..32741590hg38UCSC Ensembl
Outerchr3:32781767..32783082hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000797
SamplesKWB1
Known GenesCNOT10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149497
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