A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682595



Internal ID15072561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6990829..6990984hg38UCSC Ensembl
Innerchr16:7040830..7040985hg19UCSC Ensembl
Innerchr16:6980831..6980986hg18UCSC Ensembl
Innerchr16:6980831..6980986hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38156
hg19156
hg18156
hg17156
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515947
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682595
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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