A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655463



Internal ID18607058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168165463hg38UCSC Ensembl
Innerchr6:168335278..168566143hg19UCSC Ensembl
Innerchr6:168078127..168308992hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38230866
hg19230866
hg18230866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029722
Supporting Variants
Samples
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655463
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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