A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045237



Internal ID19134456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50402424..50528250hg38UCSC Ensembl
Innerchr13:50976560..51102386hg19UCSC Ensembl
Innerchr13:49874561..50000387hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38125827
hg19125827
hg18125827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523459
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)nsv1045237
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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