A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600061



Internal ID16387470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152144649hg38UCSC Ensembl
Innerchr5:151514956..151524210hg19UCSC Ensembl
Innerchr5:151495149..151504403hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg389255
hg199255
hg189255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10132n54
Supporting Variantsnssv1043964, nssv1043968, nssv1043970, nssv1043966, nssv1043969, nssv1043967, nssv1043965
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600061
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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