A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570839



Internal ID16358248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101251057..101252467hg38UCSC Ensembl
Innerchr15:101791262..101792672hg19UCSC Ensembl
Innerchr15:99608785..99610195hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381411
hg191411
hg181411
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851060, nssv851057, nssv851044, nssv851052, nssv851043, nssv851050, nssv851049, nssv851054, nssv851046, nssv851063, nssv851038, nssv851048, nssv851037, nssv851059, nssv851047, nssv851033, nssv851061, nssv851040, nssv851041, nssv851039, nssv851056, nssv851053, nssv851045, nssv851062, nssv851034, nssv851032, nssv851051, nssv851035, nssv851036, nssv851058, nssv851055, nssv851042
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570839
Frequency
Sample Size17421
Observed Gain29
Observed Loss3
Observed Complex0
Frequencyn/a


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