A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025324



Internal ID19114542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:346085..379003hg38UCSC Ensembl
Innerchr6:346085..379003hg19UCSC Ensembl
Innerchr6:291085..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3832919
hg1932919
hg1832919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5902n100
Supporting Variantsnssv3654650
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)nsv1025324
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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