A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520695



Internal ID15101302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6592195..6611691hg38UCSC Ensembl
Innerchr16:6642196..6661692hg19UCSC Ensembl
Innerchr16:6582197..6601693hg18UCSC Ensembl
Innerchr16:6582197..6601693hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3819497
hg1919497
hg1819497
hg1719497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674196, nssv677694
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520695
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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