A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3653569



Internal ID18951850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..378703hg38UCSC Ensembl
Innerchr6:264744..378703hg19UCSC Ensembl
Innerchr6:209744..323703hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38113960
hg19113960
hg18113960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028191
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)nssv3653569
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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