A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046915



Internal ID19136134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:79121692..79182821hg38UCSC Ensembl
Innerchr13:79695827..79756956hg19UCSC Ensembl
Innerchr13:78593828..78654957hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3861130
hg1961130
hg1861130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530518
Samples
Known GenesMIR548A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046915
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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