A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051518



Internal ID19140737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104772904..104795567hg38UCSC Ensembl
Innerchr13:105425255..105447918hg19UCSC Ensembl
Innerchr13:104223256..104245919hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3822664
hg1922664
hg1822664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n100
Supporting Variantsnssv3525552
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)nsv1051518
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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