A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615949



Internal ID16056672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136106764..136233010hg38UCSC Ensembl
Innerchr9:138998610..139124856hg19UCSC Ensembl
Innerchr9:138138431..138264677hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38126247
hg19126247
hg18126247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13001n54
Supporting Variantsnssv1148290
Samples
Known GenesC9orf69, LHX3, QSOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615949
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