A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551754



Internal ID16339163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84371303..84502050hg38UCSC Ensembl
Innerchr10:86131059..86261806hg19UCSC Ensembl
Innerchr10:86121039..86251786hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38130748
hg19130748
hg18130748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752184
Samples
Known GenesCCSER2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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