A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047276



Internal ID19136495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39160951..39265120hg38UCSC Ensembl
Innerchr13:39735088..39839257hg19UCSC Ensembl
Innerchr13:38633088..38737257hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38104170
hg19104170
hg18104170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1632n100
Supporting Variantsnssv3523385
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)nsv1047276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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