A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698851



Internal ID15435503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24507296..24520397hg38UCSC Ensembl
Innerchr16:24518617..24531718hg19UCSC Ensembl
Innerchr16:24426118..24439219hg18UCSC Ensembl
Innerchr16:24426118..24439219hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3813102
hg1913102
hg1813102
hg1713102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698851
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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