A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052329



Internal ID19141548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125992377..126072015hg38UCSC Ensembl
Innerchr9:128754656..128834294hg19UCSC Ensembl
Innerchr9:127794477..127874115hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3879639
hg1979639
hg1879639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7716n100
Supporting Variantsnssv3695237
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052329
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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