A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019802



Internal ID19109020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:254255..355524hg38UCSC Ensembl
Innerchr6:254255..355524hg19UCSC Ensembl
Innerchr6:199255..300524hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38101270
hg19101270
hg18101270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3650439
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019802
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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