A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605441



Internal ID16392850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167958531..168132968hg38UCSC Ensembl
Innerchr6:168359211..168533648hg19UCSC Ensembl
Innerchr6:168102060..168276497hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38174438
hg19174438
hg18174438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11063n54
Supporting Variantsnssv1077280
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)nsv605441
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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