A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552313



Internal ID15993036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128101314..128109477hg38UCSC Ensembl
Innerchr10:129899578..129907741hg19UCSC Ensembl
Innerchr10:129789568..129797731hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg388164
hg198164
hg188164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760517
Samples
Known GenesMKI67
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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