A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672107



Internal ID15408759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3207868..3251897hg38UCSC Ensembl
Innerchr16:3257868..3301897hg19UCSC Ensembl
Innerchr16:3197869..3241898hg18UCSC Ensembl
Innerchr16:3197869..3241898hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844030
hg1944030
hg1844030
hg1744030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516280
Supporting Variants
Samples
Known GenesMEFV, OR1F2P, ZNF200
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672107
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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