A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550859



Internal ID15991582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51444749..51451689hg38UCSC Ensembl
Innerchr10:53204509..53211449hg19UCSC Ensembl
Innerchr10:52874515..52881455hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386941
hg196941
hg186941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1131n54
Supporting Variantsnssv747832, nssv747831
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550859
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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