A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018684



Internal ID18761217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88552751..88859852hg38UCSC Ensembl
Innerchr6:89262470..89569571hg19UCSC Ensembl
Innerchr6:89319189..89626290hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38307102
hg19307102
hg18307102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6087n100
Supporting Variantsnssv3750123
Samples
Known GenesRNGTT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018684
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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