A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527027



Internal ID15454320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:68734180..68736595hg38UCSC Ensembl
Innerchr5:68030007..68032422hg19UCSC Ensembl
Innerchr5:68065763..68068178hg18UCSC Ensembl
Innerchr5:68065763..68068178hg17UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg382416
hg192416
hg182416
hg172416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527027
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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