A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570847



Internal ID16358256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101251154..101253446hg38UCSC Ensembl
Innerchr15:101791359..101793651hg19UCSC Ensembl
Innerchr15:99608882..99611174hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382293
hg192293
hg182293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n54
Supporting Variantsnssv851073
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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