A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053550



Internal ID19142769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54773815..54832407hg38UCSC Ensembl
Innerchr13:55347950..55406542hg19UCSC Ensembl
Innerchr13:54245951..54304543hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3858593
hg1958593
hg1858593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523860
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053550
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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