A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703481



Internal ID15093447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6368883..6370925hg38UCSC Ensembl
Innerchr16:6418884..6420926hg19UCSC Ensembl
Innerchr16:6358885..6360927hg18UCSC Ensembl
Innerchr16:6358885..6360927hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg382043
hg192043
hg182043
hg172043
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527101
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703481
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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