A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033616



Internal ID19122837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..376925hg38UCSC Ensembl
Innerchr6:302294..376925hg19UCSC Ensembl
Innerchr6:247294..321925hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3874632
hg1974632
hg1874632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3653742, nssv3653741, nssv3653740, nssv3653739, nssv3653743
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)nsv1033616
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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