A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036036



Internal ID19125255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26459403..26494236hg38UCSC Ensembl
Innerchr13:27033540..27068373hg19UCSC Ensembl
Innerchr13:25931540..25966373hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3834834
hg1934834
hg1834834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1622n100
Supporting Variantsnssv3523210, nssv3523211
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)nsv1036036
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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