A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023067



Internal ID19112284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:265101..294825hg38UCSC Ensembl
Innerchr6:265101..294825hg19UCSC Ensembl
Innerchr6:210101..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3829725
hg1929725
hg1829725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5879n100
Supporting Variantsnssv3653617, nssv3653610, nssv3653616, nssv3653609, nssv3653612, nssv3653614, nssv3653611, nssv3653613, nssv3653615
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)nsv1023067
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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