A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028693



Internal ID19117911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..294825hg38UCSC Ensembl
Innerchr6:264744..294825hg19UCSC Ensembl
Innerchr6:209744..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3830082
hg1930082
hg1830082
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653534, nssv3653529, nssv3653530, nssv3653522, nssv3653524, nssv3747774, nssv3653519, nssv3652767, nssv3653507, nssv3747776, nssv3747777, nssv3653515, nssv3653511, nssv3653508, nssv3653538, nssv3652766, nssv3652765, nssv3653521, nssv3653532, nssv3653526, nssv3653528, nssv3653525, nssv3747775, nssv3653510, nssv3653533, nssv3653517, nssv3747778, nssv3653523, nssv3653516, nssv3653512, nssv3653509, nssv3653518, nssv3653514, nssv3653520, nssv3653535, nssv3747779, nssv3747773, nssv3652768, nssv3653513, nssv3653539, nssv3653537, nssv3653536, nssv3653527, nssv3653531
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)nsv1028693
Frequency
Sample Size11257
Observed Gain1
Observed Loss43
Observed Complex0
Frequencyn/a


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