A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527583



Internal ID15108190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32126644..35710856hg38UCSC Ensembl
Innerchr16:32137965..34945227hg19UCSC Ensembl
Innerchr16:32045466..34802728hg18UCSC Ensembl
Innerchr16:32045466..34802728hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg383584213
hg192807263
hg182757263
hg172757263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704044
Samples
Known GenesHERC2P4, LINC00273, LOC100130700, LOC146481, LOC283914, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D, UBE2MP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527583
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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