A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522097



Internal ID15449390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:96012082..96089495hg38UCSC Ensembl
Innerchr5:95347786..95425199hg19UCSC Ensembl
Innerchr5:95373542..95450955hg18UCSC Ensembl
Innerchr5:95373542..95450955hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3877414
hg1977414
hg1877414
hg1777414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv348n21
Supporting Variantsnssv694869
Samples
Known GenesMIR583
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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