A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019405



Internal ID19108623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..381137hg38UCSC Ensembl
Innerchr6:260364..381137hg19UCSC Ensembl
Innerchr6:205364..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38120774
hg19120774
hg18120774
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652758, nssv3652757, nssv3747765, nssv3747771, nssv3747769, nssv3652756, nssv3747766, nssv3747767, nssv3652755, nssv3747768, nssv3747770
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)nsv1019405
Frequency
Sample Size11257
Observed Gain4
Observed Loss7
Observed Complex0
Frequencyn/a


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