A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550858



Internal ID15991581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51444749..51449614hg38UCSC Ensembl
Innerchr10:53204509..53209374hg19UCSC Ensembl
Innerchr10:52874515..52879380hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384866
hg194866
hg184866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747830
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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