A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570593



Internal ID16358002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97265448..97320421hg38UCSC Ensembl
Innerchr15:97808678..97863651hg19UCSC Ensembl
Innerchr15:95609682..95664655hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3854974
hg1954974
hg1854974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4747n54
Supporting Variantsnssv849143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570593
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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