A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029895



Internal ID19119114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:290586..379003hg38UCSC Ensembl
Innerchr6:290586..379003hg19UCSC Ensembl
Innerchr6:235586..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3888418
hg1988418
hg1888418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5888n100
Supporting Variantsnssv3653693, nssv3653692
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)nsv1029895
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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