A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006146



Internal ID18748677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158758035..158907989hg38UCSC Ensembl
Innerchr3:158475824..158625778hg19UCSC Ensembl
Innerchr3:159958518..160108472hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38149955
hg19149955
hg18149955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606398
Samples
Known GenesMFSD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006146
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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