A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052841



Internal ID18795372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101611117..101672732hg38UCSC Ensembl
Innerchr15:102151320..102212935hg19UCSC Ensembl
Innerchr15:99968843..100030458hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3861616
hg1961616
hg1861616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2679n100
Supporting Variantsnssv3555377
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)nsv1052841
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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