A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519909



Internal ID15447202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19027882..19033378hg38UCSC Ensembl
Innerchr9:19027880..19033376hg19UCSC Ensembl
Innerchr9:19017880..19023376hg18UCSC Ensembl
Innerchr9:19017880..19023376hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg385497
hg195497
hg185497
hg175497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659447, nssv663408
Samples
Known GenesFAM154A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519909
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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