A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550876



Internal ID15991599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52104642..52189094hg38UCSC Ensembl
Innerchr10:53864402..53948854hg19UCSC Ensembl
Innerchr10:53534408..53618860hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3884453
hg1984453
hg1884453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747855
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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