A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551671



Internal ID16339080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81678671..81749799hg38UCSC Ensembl
Innerchr10:83438427..83509555hg19UCSC Ensembl
Innerchr10:83428407..83499535hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3871129
hg1971129
hg1871129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1298n54
Supporting Variantsnssv1174556
Samples1780862042_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551671
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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