A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015536



Internal ID19104753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:294274..381137hg38UCSC Ensembl
Innerchr6:294274..381137hg19UCSC Ensembl
Innerchr6:239274..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3886864
hg1986864
hg1886864
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5890n100
Supporting Variantsnssv3653709, nssv3747822, nssv3747820, nssv3747823, nssv3653708, nssv3653707, nssv3747821
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)nsv1015536
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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