A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655499



Internal ID18607094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168195239hg38UCSC Ensembl
Innerchr6:168335278..168595919hg19UCSC Ensembl
Innerchr6:168078127..168338768hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38260642
hg19260642
hg18260642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033241
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)nssv3655499
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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