A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521783



Internal ID15102390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104757168..104770036hg38UCSC Ensembl
Innerchr9:107519449..107532317hg19UCSC Ensembl
Innerchr9:106559270..106572138hg18UCSC Ensembl
Innerchr9:104599004..104611872hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3812869
hg1912869
hg1812869
hg1712869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694551
Samples
Known GenesNIPSNAP3A, NIPSNAP3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521783
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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