A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019041



Internal ID19108258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..385772hg38UCSC Ensembl
Innerchr6:302294..385772hg19UCSC Ensembl
Innerchr6:247294..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3883479
hg1983479
hg1883479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3653820, nssv3653819, nssv3653821, nssv3653822
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)nsv1019041
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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