A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062565



Internal ID19151784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:66113391..66224832hg38UCSC Ensembl
Innerchr16:66147294..66258735hg19UCSC Ensembl
Innerchr16:64704795..64816236hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38111442
hg19111442
hg18111442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722725
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)nsv1062565
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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