A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700814



Internal ID15090780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7598266..7598443hg38UCSC Ensembl
Innerchr16:7648268..7648445hg19UCSC Ensembl
Innerchr16:7588269..7588446hg18UCSC Ensembl
Innerchr16:7588269..7588446hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38178
hg19178
hg18178
hg17178
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524819
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700814
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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