A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551841



Internal ID15992564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88999967..89015999hg38UCSC Ensembl
Innerchr10:90759724..90775756hg19UCSC Ensembl
Innerchr10:90749704..90765736hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3816033
hg1916033
hg1816033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753224
Samples
Known GenesFAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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