A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017166



Internal ID18759701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145355935..145487312hg38UCSC Ensembl
Innerchr6:145677071..145808448hg19UCSC Ensembl
Innerchr6:145718764..145850141hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38131378
hg19131378
hg18131378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749558
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017166
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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