A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570826



Internal ID16011549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100879954..100883261hg38UCSC Ensembl
Innerchr15:101420159..101423466hg19UCSC Ensembl
Innerchr15:99237682..99240989hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg383308
hg193308
hg183308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851017
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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