A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660102



Internal ID15050068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7355610..7421605hg38UCSC Ensembl
Innerchr16:7405611..7471606hg19UCSC Ensembl
Innerchr16:7345612..7411607hg18UCSC Ensembl
Innerchr16:7345612..7411607hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3865996
hg1965996
hg1865996
hg1765996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520018
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660102
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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