A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051185



Internal ID19140404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83931762..83990097hg38UCSC Ensembl
Innerchr13:84505897..84564232hg19UCSC Ensembl
Innerchr13:83403898..83462233hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3858336
hg1958336
hg1858336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525405
Samples
Known GenesMIR548F1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051185
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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