A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045826



Internal ID19135045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46944467..47001133hg38UCSC Ensembl
Innerchr15:47236665..47293331hg19UCSC Ensembl
Innerchr15:45023957..45080623hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3856667
hg1956667
hg1856667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552373
Samples
Known GenesMIR548A3, MIR548U
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045826
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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