A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551793



Internal ID16339202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86658778..86682683hg38UCSC Ensembl
Innerchr10:88418535..88442440hg19UCSC Ensembl
Innerchr10:88408515..88432420hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3823906
hg1923906
hg1823906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1321n54
Supporting Variantsnssv1174565
SamplesHGDP00546
Known GenesLDB3, OPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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