A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551826



Internal ID16339235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87513822..87516650hg38UCSC Ensembl
Innerchr10:89273579..89276407hg19UCSC Ensembl
Innerchr10:89263559..89266387hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382829
hg192829
hg182829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752276
Samples
Known GenesMINPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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