A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029211



Internal ID19118430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:265101..381137hg38UCSC Ensembl
Innerchr6:265101..381137hg19UCSC Ensembl
Innerchr6:210101..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38116037
hg19116037
hg18116037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653624, nssv3653623, nssv3653622, nssv3653621
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)nsv1029211
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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