A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605429



Internal ID16392838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167948331..168191454hg38UCSC Ensembl
Innerchr6:168349011..168592134hg19UCSC Ensembl
Innerchr6:168091860..168334983hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38243124
hg19243124
hg18243124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11062n54
Supporting Variantsnssv1077264, nssv1077263
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605429
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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