A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516897



Internal ID15444190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104051184..104088570hg38UCSC Ensembl
Innerchr9:106813465..106850851hg19UCSC Ensembl
Innerchr9:105853286..105890672hg18UCSC Ensembl
Innerchr9:103893020..103930406hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3837387
hg1937387
hg1837387
hg1737387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673263, nssv661459, nssv654743, nssv690026, nssv681136
Samples
Known GenesMIR6130
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516897
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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