A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605399



Internal ID16046122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168149315hg38UCSC Ensembl
Innerchr6:168342776..168549995hg19UCSC Ensembl
Innerchr6:168085625..168292844hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38207220
hg19207220
hg18207220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11063n54
Supporting Variantsnssv1077213
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)nsv605399
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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