A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600358



Internal ID16387767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177068100..177071881hg38UCSC Ensembl
Innerchr5:176495101..176498882hg19UCSC Ensembl
Innerchr5:176427707..176431488hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg383782
hg193782
hg183782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045721
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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