A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019741



Internal ID19108959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314950..381137hg38UCSC Ensembl
Innerchr6:314950..381137hg19UCSC Ensembl
Innerchr6:259950..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866188
hg1966188
hg1866188
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5896n100
Supporting Variantsnssv3653841, nssv3653843, nssv3653851, nssv3747884, nssv3653842, nssv3653845, nssv3653844, nssv3653848, nssv3653846, nssv3653840, nssv3653847, nssv3747882, nssv3653849, nssv3653850, nssv3747883
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)nsv1019741
Frequency
Sample Size11257
Observed Gain9
Observed Loss6
Observed Complex0
Frequencyn/a


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