A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021268



Internal ID19110485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:279695..381137hg38UCSC Ensembl
Innerchr6:279695..381137hg19UCSC Ensembl
Innerchr6:224695..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38101443
hg19101443
hg18101443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653667
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)nsv1021268
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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