A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552022



Internal ID16339431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95548357..95568470hg38UCSC Ensembl
Innerchr10:97308114..97328227hg19UCSC Ensembl
Innerchr10:97298104..97318217hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3820114
hg1920114
hg1820114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756033
Samples
Known GenesSORBS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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