A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046535



Internal ID18789066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31059860..31099938hg38UCSC Ensembl
Innerchr15:31352063..31392141hg19UCSC Ensembl
Innerchr15:29139355..29179433hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3840079
hg1940079
hg1840079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2534n100
Supporting Variantsnssv3547652
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046535
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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