A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551755



Internal ID16339164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84570457..84592655hg38UCSC Ensembl
Innerchr10:86330213..86352411hg19UCSC Ensembl
Innerchr10:86320193..86342391hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3822199
hg1922199
hg1822199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752185
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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