A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605397



Internal ID16046120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168137838hg38UCSC Ensembl
Innerchr6:168342776..168538518hg19UCSC Ensembl
Innerchr6:168085625..168281367hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38195743
hg19195743
hg18195743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11063n54
Supporting Variantsnssv1077211
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)nsv605397
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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