A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694795



Internal ID15084761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6627776..6663776hg38UCSC Ensembl
Innerchr16:6677777..6713777hg19UCSC Ensembl
Innerchr16:6617778..6653778hg18UCSC Ensembl
Innerchr16:6617778..6653778hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3836001
hg1936001
hg1836001
hg1736001
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522025
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694795
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer