A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051619



Internal ID19140838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54991608..55465444hg38UCSC Ensembl
Innerchr13:55565743..56039579hg19UCSC Ensembl
Innerchr13:54463744..54937580hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38473837
hg19473837
hg18473837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714988
Samples
Known GenesMIR5007
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051619
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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