A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570846



Internal ID16358255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101251154..101253363hg38UCSC Ensembl
Innerchr15:101791359..101793568hg19UCSC Ensembl
Innerchr15:99608882..99611091hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382210
hg192210
hg182210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n54
Supporting Variantsnssv851072, nssv851071
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570846
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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