A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599357



Internal ID16386766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110991768..111035989hg38UCSC Ensembl
Innerchr5:110327467..110371687hg19UCSC Ensembl
Innerchr5:110355366..110399586hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3844222
hg1944221
hg1844221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1040248
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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