A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614554



Internal ID16401963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69126301..69127886hg38UCSC Ensembl
Innerchr9:71741217..71742802hg19UCSC Ensembl
Innerchr9:70931037..70932622hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381586
hg191586
hg181586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12739n54
Supporting Variantsnssv1134769, nssv1134767, nssv1134771, nssv1134773, nssv1134768, nssv1134766, nssv1134772, nssv1134774, nssv1134775, nssv1134777, nssv1134776, nssv1134770
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614554
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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