A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009745



Internal ID18752276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46738588..46808087hg38UCSC Ensembl
Innerchr3:46780078..46849577hg19UCSC Ensembl
Innerchr3:46755082..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3869500
hg1969500
hg1869500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4730n100
Supporting Variantsnssv3589746, nssv3589747, nssv3589745, nssv3589749, nssv3589748
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)nsv1009745
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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