A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048106



Internal ID19137325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81325867..81344862hg38UCSC Ensembl
Innerchr15:81618208..81637203hg19UCSC Ensembl
Innerchr15:79405263..79424258hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3818996
hg1918996
hg1818996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554596
Samples
Known GenesTMC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048106
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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