A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593775



Internal ID18545370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46838650hg38UCSC Ensembl
Innerchr3:46801805..46880140hg19UCSC Ensembl
Innerchr3:46776809..46855144hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3878336
hg1978336
hg1878336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004452
Supporting Variants
Samples
Known GenesPRSS42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3593775
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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