A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528797



Internal ID15109404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104919731..104920841hg38UCSC Ensembl
Innerchr9:107682012..107683122hg19UCSC Ensembl
Innerchr9:106721833..106722943hg18UCSC Ensembl
Innerchr9:104761567..104762677hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381111
hg191111
hg181111
hg171111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705470
Samples
Known GenesABCA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528797
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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