A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552298



Internal ID16339707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127048956..127058288hg38UCSC Ensembl
Innerchr10:128847220..128856552hg19UCSC Ensembl
Innerchr10:128737210..128746542hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg389333
hg199333
hg189333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760497
Samples
Known GenesDOCK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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