A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008803



Internal ID18751334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46741757..46807677hg38UCSC Ensembl
Innerchr3:46783247..46849167hg19UCSC Ensembl
Innerchr3:46758251..46824171hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3865921
hg1965921
hg1865921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4730n100
Supporting Variantsnssv3590870, nssv3590873, nssv3590872, nssv3590869, nssv3590871
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)nsv1008803
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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