A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549912



Internal ID15990635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6525013..6587263hg38UCSC Ensembl
Innerchr10:6566975..6629225hg19UCSC Ensembl
Innerchr10:6606981..6669231hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3862251
hg1962251
hg1862251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743528
Samples
Known GenesPRKCQ, PRKCQ-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549912
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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