A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517558



Internal ID15444851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5466868..5532501hg38UCSC Ensembl
Innerchr7:5506499..5572132hg19UCSC Ensembl
Innerchr7:5473025..5538658hg18UCSC Ensembl
Innerchr7:5279740..5345373hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3865634
hg1965634
hg1865634
hg1765634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683177, nssv668497, nssv676882, nssv671533, nssv687770, nssv652355
Samples
Known GenesACTB, FBXL18, MIR589
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517558
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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