A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050429



Internal ID18792960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46672048..46758543hg38UCSC Ensembl
Innerchr15:46964246..47050741hg19UCSC Ensembl
Innerchr15:44751538..44838033hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3886496
hg1986496
hg1886496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716722
Samples
Known GenesMIR548A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050429
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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