A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054948



Internal ID19144167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26459403..26492860hg38UCSC Ensembl
Innerchr13:27033540..27066997hg19UCSC Ensembl
Innerchr13:25931540..25964997hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3833458
hg1933458
hg1833458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1622n100
Supporting Variantsnssv3523209
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)nsv1054948
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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