A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550898



Internal ID15991621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52256737..52258268hg38UCSC Ensembl
Innerchr10:54016497..54018028hg19UCSC Ensembl
Innerchr10:53686503..53688034hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381532
hg191532
hg181532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1137n54
Supporting Variantsnssv748112
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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