A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050178



Internal ID19139397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31719274..32151995hg38UCSC Ensembl
Innerchr15:32011477..32444196hg19UCSC Ensembl
Innerchr15:29798769..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38432722
hg19432720
hg18432720
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n100
Supporting Variantsnssv3547685, nssv3547684, nssv3547681, nssv3547676, nssv3547679, nssv3547678, nssv3721592, nssv3721594, nssv3721595, nssv3547675, nssv3547683, nssv3547680, nssv3547677, nssv3547682, nssv3721593
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050178
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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