A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655457



Internal ID18607052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167930902..168195239hg38UCSC Ensembl
Innerchr6:168331582..168595919hg19UCSC Ensembl
Innerchr6:168074431..168338768hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38264338
hg19264338
hg18264338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016877
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)nssv3655457
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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