A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551844



Internal ID16339253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89119547..89139687hg38UCSC Ensembl
Innerchr10:90879304..90899444hg19UCSC Ensembl
Innerchr10:90869284..90889424hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3820141
hg1920141
hg1820141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753227
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551844
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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