A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525006



Internal ID15105613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6793830..6794094hg38UCSC Ensembl
Innerchr16:6843831..6844095hg19UCSC Ensembl
Innerchr16:6783832..6784096hg18UCSC Ensembl
Innerchr16:6783832..6784096hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38265
hg19265
hg18265
hg17265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701041
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525006
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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