A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022444



Internal ID19111662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..382897hg38UCSC Ensembl
Innerchr6:302294..382897hg19UCSC Ensembl
Innerchr6:247294..327897hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3880604
hg1980604
hg1880604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3653816, nssv3653812, nssv3653814, nssv3747874, nssv3653809, nssv3653811, nssv3653810, nssv3653815, nssv3653813, nssv3747875
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)nsv1022444
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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