A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053474



Internal ID18796005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101612385..101675562hg38UCSC Ensembl
Innerchr15:102152588..102215765hg19UCSC Ensembl
Innerchr15:99970111..100033288hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3863178
hg1963178
hg1863178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2679n100
Supporting Variantsnssv3555378, nssv3555379, nssv3718227
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053474
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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