A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526537



Internal ID15107144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7095566..7103691hg38UCSC Ensembl
Innerchr16:7145567..7153692hg19UCSC Ensembl
Innerchr16:7085568..7093693hg18UCSC Ensembl
Innerchr16:7085568..7093693hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg388126
hg198126
hg188126
hg178126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702851
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526537
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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