A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3652496



Internal ID18950777
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 loss
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)nssv3652496
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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