A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570811



Internal ID16358220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879147..100880322hg38UCSC Ensembl
Innerchr15:101419352..101420527hg19UCSC Ensembl
Innerchr15:99236875..99238050hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381176
hg191176
hg181176
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4783n54
Supporting Variantsnssv850986, nssv850977, nssv850987, nssv850984, nssv850979, nssv850978, nssv850976, nssv850983, nssv850981, nssv850975, nssv850988, nssv850982, nssv850980, nssv850985
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570811
Frequency
Sample Size17421
Observed Gain13
Observed Loss1
Observed Complex0
Frequencyn/a


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