A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570202



Internal ID16010925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78622903..78661443hg38UCSC Ensembl
Innerchr15:78915245..78953785hg19UCSC Ensembl
Innerchr15:76702300..76740840hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3838541
hg1938541
hg1838541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847446
Samples
Known GenesCHRNB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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