A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527028



Internal ID15107635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35557209..35574612hg38UCSC Ensembl
Innerchr9:35557206..35574609hg19UCSC Ensembl
Innerchr9:35547206..35564609hg18UCSC Ensembl
Innerchr9:35547206..35564609hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3817404
hg1917404
hg1817404
hg1717404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703403
Samples
Known GenesFAM166B, RUSC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527028
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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