A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614825



Internal ID16402234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89058556..89060112hg38UCSC Ensembl
Innerchr9:91673471..91675027hg19UCSC Ensembl
Innerchr9:90863291..90864847hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381557
hg191557
hg181557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139219
Samples
Known GenesSHC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614825
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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