A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077215



Internal ID15930401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168176780hg38UCSC Ensembl
Innerchr6:168342776..168577460hg19UCSC Ensembl
Innerchr6:168085625..168320309hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38234685
hg19234685
hg18234685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605401
Supporting Variants
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)nssv1077215
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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