A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018010



Internal ID19107227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..302294hg38UCSC Ensembl
Innerchr6:257341..302294hg19UCSC Ensembl
Innerchr6:202341..247294hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3844954
hg1944954
hg1844954
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3651483, nssv3651484, nssv3651480, nssv3651482, nssv3651485, nssv3651481, nssv3651479
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)nsv1018010
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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