A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698227



Internal ID15088193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:430096..445538hg38UCSC Ensembl
Innerchr16:480096..495538hg19UCSC Ensembl
Innerchr16:420097..435539hg18UCSC Ensembl
Innerchr16:420097..435539hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815443
hg1915443
hg1815443
hg1715443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521610
Supporting Variants
Samples
Known GenesRAB11FIP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698227
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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