A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153476



Internal ID19201650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:32444301..32446902hg38UCSC Ensembl
Outerchr9:32444299..32446900hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001395
SamplesKWB1
Known GenesACO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153476
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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