A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015256



Internal ID18757790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149649..336797hg38UCSC Ensembl
Innerchr6:149649..336797hg19UCSC Ensembl
Innerchr6:94649..281797hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38187149
hg19187149
hg18187149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5868n100
Supporting Variantsnssv3650369
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)nsv1015256
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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