A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527980



Internal ID15455273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14345606..14348564hg38UCSC Ensembl
Innerchr9:14345605..14348563hg19UCSC Ensembl
Innerchr9:14335605..14338563hg18UCSC Ensembl
Innerchr9:14335605..14338563hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382959
hg192959
hg182959
hg172959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv480n21
Supporting Variantsnssv704498
Samples
Known GenesNFIB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527980
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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