A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605403



Internal ID16392812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167942096..168193059hg38UCSC Ensembl
Innerchr6:168342776..168593739hg19UCSC Ensembl
Innerchr6:168085625..168336588hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38250964
hg19250964
hg18250964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11062n54
Supporting Variantsnssv1077217, nssv1077221, nssv1077219, nssv1077224, nssv1077220, nssv1077218, nssv1077222, nssv1077223
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)nsv605403
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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