A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701569



Internal ID15438221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106122259..106131501hg38UCSC Ensembl
Innerchr9:108884540..108893782hg19UCSC Ensembl
Innerchr9:107924361..107933603hg18UCSC Ensembl
Innerchr9:105964095..105973337hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg389243
hg199243
hg189243
hg179243
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525441
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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