A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598959



Internal ID16386368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95620641..95627477hg38UCSC Ensembl
Innerchr5:94956345..94963181hg19UCSC Ensembl
Innerchr5:94982101..94988937hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386837
hg196837
hg186837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038109
Samples
Known GenesGPR150
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598959
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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