A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026836



Internal ID18769367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70017855..70139122hg38UCSC Ensembl
Innerchr6:70727747..70849014hg19UCSC Ensembl
Innerchr6:70784468..70905735hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38121268
hg19121268
hg18121268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658805
Samples
Known GenesCOL19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026836
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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