A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753225



Internal ID16047181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89056218..89130240hg38UCSC Ensembl
Innerchr10:90815975..90889997hg19UCSC Ensembl
Innerchr10:90805955..90879977hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3874023
hg1974023
hg1874023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551842
Supporting Variants
Samples
Known GenesMIR4679-1, MIR4679-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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