A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016091



Internal ID19105309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..294825hg38UCSC Ensembl
Innerchr6:258253..294825hg19UCSC Ensembl
Innerchr6:203253..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3836573
hg1936573
hg1836573
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3652695, nssv3652694, nssv3747738, nssv3652691, nssv3652679, nssv3652696, nssv3652697, nssv3652685, nssv3747741, nssv3747734, nssv3652681, nssv3652688, nssv3652687, nssv3747737, nssv3747736, nssv3652683, nssv3652690, nssv3652686, nssv3652689, nssv3652675, nssv3652684, nssv3652693, nssv3747735, nssv3652676, nssv3652682, nssv3652698, nssv3652699, nssv3747739, nssv3652692, nssv3652678, nssv3747740, nssv3652680, nssv3652677
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)nsv1016091
Frequency
Sample Size11257
Observed Gain3
Observed Loss30
Observed Complex0
Frequencyn/a


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