A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036318



Internal ID18778849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43761419..43868575hg38UCSC Ensembl
Innerchr15:44053617..44160773hg19UCSC Ensembl
Innerchr15:41840909..41948065hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38107157
hg19107157
hg18107157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552332
Samples
Known GenesELL3, HYPK, MFAP1, MIR1282, PDIA3, SERF2, SERF2-C15ORF63, SERINC4, WDR76
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036318
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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