A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521589



Internal ID15102196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5768328..5888325hg38UCSC Ensembl
Innerchr7:5807959..5927956hg19UCSC Ensembl
Innerchr7:5774485..5894482hg18UCSC Ensembl
Innerchr7:5581200..5701197hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38119998
hg19119998
hg18119998
hg17119998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv402n21
Supporting Variantsnssv698207
Samples
Known GenesOCM, RNF216, ZNF815P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521589
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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