A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570825



Internal ID16011548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879748..100881667hg38UCSC Ensembl
Innerchr15:101419953..101421872hg19UCSC Ensembl
Innerchr15:99237476..99239395hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381920
hg191920
hg181920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851016
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570825
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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