A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064107



Internal ID19153326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55621512..55641775hg38UCSC Ensembl
Innerchr16:55655424..55675687hg19UCSC Ensembl
Innerchr16:54212925..54233188hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3820264
hg1920264
hg1820264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559289
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)nsv1064107
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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