A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590894



Internal ID18542489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46741757..46808087hg38UCSC Ensembl
Innerchr3:46783247..46849577hg19UCSC Ensembl
Innerchr3:46758251..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3866331
hg1966331
hg1866331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008289
Supporting Variants
Samples
Known GenesPRSS45
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3590894
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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