A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015877



Internal ID19105095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..355524hg38UCSC Ensembl
Innerchr6:302294..355524hg19UCSC Ensembl
Innerchr6:247294..300524hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3853231
hg1953231
hg1853231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5893n100
Supporting Variantsnssv3653715
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)nsv1015877
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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