A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050172



Internal ID19139391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32356519hg38UCSC Ensembl
Innerchr15:32458661..32648720hg19UCSC Ensembl
Innerchr15:30245953..30436012hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38190060
hg19190060
hg18190060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3547729
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)nsv1050172
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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