A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519920



Internal ID15447213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83023704..83036514hg38UCSC Ensembl
Innerchr7:82653020..82665830hg19UCSC Ensembl
Innerchr7:82490956..82503766hg18UCSC Ensembl
Innerchr7:82297671..82310481hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3812811
hg1912811
hg1812811
hg1712811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697126
Samples
Known GenesPCLO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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