A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550959



Internal ID15991682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54476971..54526308hg38UCSC Ensembl
Innerchr10:56236731..56286068hg19UCSC Ensembl
Innerchr10:55906737..55956074hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3849338
hg1949338
hg1849338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1155n54
Supporting Variantsnssv1173895
Samples1780862176_A
Known GenesPCDH15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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