A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048746



Internal ID18791277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064523..31097745hg38UCSC Ensembl
Innerchr15:31356726..31389948hg19UCSC Ensembl
Innerchr15:29144018..29177240hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3833223
hg1933223
hg1833223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2534n100
Supporting Variantsnssv3721587, nssv3547653
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)nsv1048746
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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