A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551845



Internal ID16339254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89159378..89204269hg38UCSC Ensembl
Innerchr10:90919135..90964026hg19UCSC Ensembl
Innerchr10:90909115..90954006hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3844892
hg1944892
hg1844892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753228, nssv753229
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551845
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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