A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528933



Internal ID15456226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99022495..99026240hg38UCSC Ensembl
Innerchr9:101784777..101788522hg19UCSC Ensembl
Innerchr9:100824598..100828343hg18UCSC Ensembl
Innerchr9:98864332..98868077hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383746
hg193746
hg183746
hg173746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705624
Samples
Known GenesCOL15A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528933
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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