A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524873



Internal ID15452166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3201522..3204470hg38UCSC Ensembl
Innerchr16:3251522..3254470hg19UCSC Ensembl
Innerchr16:3191523..3194471hg18UCSC Ensembl
Innerchr16:3191523..3194471hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382949
hg192949
hg182949
hg172949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700878
Samples
Known GenesOR1F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524873
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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