A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030097



Internal ID18772628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:249798..381137hg38UCSC Ensembl
Innerchr6:249798..381137hg19UCSC Ensembl
Innerchr6:194798..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38131340
hg19131340
hg18131340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5872n100
Supporting Variantsnssv3650391, nssv3650390
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)nsv1030097
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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