A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699694



Internal ID15089660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88601643..88635372hg38UCSC Ensembl
Innerchr16:88668051..88701780hg19UCSC Ensembl
Innerchr16:87195552..87229281hg18UCSC Ensembl
Innerchr16:87195552..87229281hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3833730
hg1933730
hg1833730
hg1733730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523859
Supporting Variants
Samples
Known GenesZC3H18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699694
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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