A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701620



Internal ID15091586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65252967..65305991hg38UCSC Ensembl
Innerchr16:65286870..65339894hg19UCSC Ensembl
Innerchr16:63844371..63897395hg18UCSC Ensembl
Innerchr16:63844371..63897395hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3853025
hg1953025
hg1853025
hg1753025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525489
Supporting Variants
Samples
Known GenesLINC00922
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701620
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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