A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551857



Internal ID16339266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89180930..89204638hg38UCSC Ensembl
Innerchr10:90940687..90964395hg19UCSC Ensembl
Innerchr10:90930667..90954375hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3823709
hg1923709
hg1823709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1335n54
Supporting Variantsnssv753300, nssv753298, nssv753299, nssv753296, nssv753297, nssv753295, nssv753294
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551857
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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