A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016869



Internal ID19106086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..303121hg38UCSC Ensembl
Innerchr6:260364..303121hg19UCSC Ensembl
Innerchr6:205364..248121hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842758
hg1942758
hg1842758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5886n100
Supporting Variantsnssv3747760, nssv3652739, nssv3652740, nssv3652741
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)nsv1016869
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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