A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3653690



Internal ID18951971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:290586..366333hg38UCSC Ensembl
Innerchr6:290586..366333hg19UCSC Ensembl
Innerchr6:235586..311333hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3875748
hg1975748
hg1875748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032728
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)nssv3653690
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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