A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570832



Internal ID16358241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101166509..101177683hg38UCSC Ensembl
Innerchr15:101706714..101717888hg19UCSC Ensembl
Innerchr15:99524237..99535411hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3811175
hg1911175
hg1811175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4788n54
Supporting Variantsnssv851024
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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