A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000774



Internal ID18743305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46836636hg38UCSC Ensembl
Innerchr3:46801805..46878126hg19UCSC Ensembl
Innerchr3:46776809..46853130hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3876322
hg1976322
hg1876322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4732n100
Supporting Variantsnssv3593774
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)nsv1000774
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer