A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522448



Internal ID15449741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86057292..86057465hg38UCSC Ensembl
Innerchr16:86090898..86091071hg19UCSC Ensembl
Innerchr16:84648399..84648572hg18UCSC Ensembl
Innerchr16:84648399..84648572hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38174
hg19174
hg18174
hg17174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705807
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522448
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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