A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029144



Internal ID19118363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:279695..384546hg38UCSC Ensembl
Innerchr6:279695..384546hg19UCSC Ensembl
Innerchr6:224695..329546hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38104852
hg19104852
hg18104852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653669, nssv3653668
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)nsv1029144
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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