A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022368



Internal ID19111586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:269735..381137hg38UCSC Ensembl
Innerchr6:269735..381137hg19UCSC Ensembl
Innerchr6:214735..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38111403
hg19111403
hg18111403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3747799, nssv3653657, nssv3747800
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)nsv1022368
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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