A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605396



Internal ID16046119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168133107hg38UCSC Ensembl
Innerchr6:168342776..168533787hg19UCSC Ensembl
Innerchr6:168085625..168276636hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38191012
hg19191012
hg18191012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11063n54
Supporting Variantsnssv1077210
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)nsv605396
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