A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551827



Internal ID16339236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87513822..87516942hg38UCSC Ensembl
Innerchr10:89273579..89276699hg19UCSC Ensembl
Innerchr10:89263559..89266679hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg383121
hg193121
hg183121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752277
Samples
Known GenesMINPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551827
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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