A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026036



Internal ID19115253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..303121hg38UCSC Ensembl
Innerchr6:264744..303121hg19UCSC Ensembl
Innerchr6:209744..248121hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3747780, nssv3653549, nssv3653543, nssv3653547, nssv3653544, nssv3653550, nssv3653542, nssv3653546, nssv3653548, nssv3653545
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)nsv1026036
Frequency
Sample Size11257
Observed Gain1
Observed Loss9
Observed Complex0
Frequencyn/a


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