A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598954



Internal ID16039677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95447471..95523895hg38UCSC Ensembl
Innerchr5:94783175..94859599hg19UCSC Ensembl
Innerchr5:94808931..94885355hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3876425
hg1976425
hg1876425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038098
Samples
Known GenesFAM81B, TTC37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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