A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019422



Internal ID18761957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13621911..13694549hg38UCSC Ensembl
Innerchr6:13622143..13694781hg19UCSC Ensembl
Innerchr6:13730122..13802760hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3872639
hg1972639
hg1872639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654790
Samples
Known GenesRANBP9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019422
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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