A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019063



Internal ID19108280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:267610..356249hg38UCSC Ensembl
Innerchr6:267610..356249hg19UCSC Ensembl
Innerchr6:212610..301249hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3888640
hg1988640
hg1888640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3653634
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)nsv1019063
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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