A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134153



Internal ID15987339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66791121..66955365hg38UCSC Ensembl
Innerchr9:40737476..40901750hg19UCSC Ensembl
Innerchr9:40727476..40891750hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38164245
hg19164275
hg18164275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614323
Supporting Variants
Samples
Known GenesZNF658
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134153
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