A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055982



Internal ID18798513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80117707..80169026hg38UCSC Ensembl
Innerchr16:80151604..80202923hg19UCSC Ensembl
Innerchr16:78709105..78760424hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3851320
hg1951320
hg1851320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559779
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055982
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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