A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525921



Internal ID15106528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6704527..6706395hg38UCSC Ensembl
Innerchr16:6754528..6756396hg19UCSC Ensembl
Innerchr16:6694529..6696397hg18UCSC Ensembl
Innerchr16:6694529..6696397hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381869
hg191869
hg181869
hg171869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702125
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525921
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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