A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650386



Internal ID18948667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:249798..331867hg38UCSC Ensembl
Innerchr6:249798..331867hg19UCSC Ensembl
Innerchr6:194798..276867hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3882070
hg1982070
hg1882070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030110
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)nssv3650386
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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