A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053983



Internal ID19143202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54628652..54706985hg38UCSC Ensembl
Innerchr15:54920850..54999183hg19UCSC Ensembl
Innerchr15:52708142..52786475hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3878334
hg1978334
hg1878334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552437
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)nsv1053983
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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