A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552312



Internal ID15993035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128091905..128108100hg38UCSC Ensembl
Innerchr10:129890169..129906364hg19UCSC Ensembl
Innerchr10:129780159..129796354hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3816196
hg1916196
hg1816196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174583
SamplesNINDS_54
Known GenesMKI67
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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