A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023143



Internal ID19112360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..361143hg38UCSC Ensembl
Innerchr6:258253..361143hg19UCSC Ensembl
Innerchr6:203253..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38102891
hg19102891
hg18102891
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652713, nssv3652711, nssv3652715, nssv3652714, nssv3652712
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)nsv1023143
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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