A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747724



Internal ID19046005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..381137hg38UCSC Ensembl
Innerchr6:257341..381137hg19UCSC Ensembl
Innerchr6:202341..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38123797
hg19123797
hg18123797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018834
Supporting Variants
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)nssv3747724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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