A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700525



Internal ID15090491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6604458..6631636hg38UCSC Ensembl
Innerchr16:6654459..6681637hg19UCSC Ensembl
Innerchr16:6594460..6621638hg18UCSC Ensembl
Innerchr16:6594460..6621638hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3827179
hg1927179
hg1827179
hg1727179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524570
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700525
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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