A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550868



Internal ID15991591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51483347..51488431hg38UCSC Ensembl
Innerchr10:53243107..53248191hg19UCSC Ensembl
Innerchr10:52913113..52918197hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg385085
hg195085
hg185085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747850
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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