A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011146



Internal ID18753680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146141235..146193642hg38UCSC Ensembl
Innerchr3:145859022..145911429hg19UCSC Ensembl
Innerchr3:147341712..147394119hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3852408
hg1952408
hg1852408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606164
Samples
Known GenesPLOD2, PLSCR4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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