A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521191



Internal ID15448484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15218949..15246654hg38UCSC Ensembl
Innerchr9:15218947..15246652hg19UCSC Ensembl
Innerchr9:15208947..15236652hg18UCSC Ensembl
Innerchr9:15208947..15236652hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3827706
hg1927706
hg1827706
hg1727706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697836
Samples
Known GenesTTC39B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521191
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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