A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030168



Internal ID19119387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167934598..168041795hg38UCSC Ensembl
Innerchr6:168335278..168442475hg19UCSC Ensembl
Innerchr6:168078127..168185324hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38107198
hg19107198
hg18107198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655459, nssv3655460
Samples
Known GenesHGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030168
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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