A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024314



Internal ID19113531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..376925hg38UCSC Ensembl
Innerchr6:257341..376925hg19UCSC Ensembl
Innerchr6:202341..321925hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38119585
hg19119585
hg18119585
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652418, nssv3652420, nssv3652422, nssv3652424, nssv3652421, nssv3747635, nssv3652419, nssv3652423, nssv3652425, nssv3652417
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)nsv1024314
Frequency
Sample Size11257
Observed Gain4
Observed Loss6
Observed Complex0
Frequencyn/a


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