A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570388



Internal ID16011111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89730911..89794962hg38UCSC Ensembl
Innerchr15:90274142..90338193hg19UCSC Ensembl
Innerchr15:88075146..88139197hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3864052
hg1964052
hg1864052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848201
Samples
Known GenesANPEP, MESP1, MESP2, WDR93
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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