A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515947



Internal ID15096554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6990829..6996257hg38UCSC Ensembl
Innerchr16:7040830..7046258hg19UCSC Ensembl
Innerchr16:6980831..6986259hg18UCSC Ensembl
Innerchr16:6980831..6986259hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg385429
hg195429
hg185429
hg175429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656279, nssv665411, nssv682595, nssv677272
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515947
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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