A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063811



Internal ID19153030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63160996..63387455hg38UCSC Ensembl
Innerchr16:63194900..63421359hg19UCSC Ensembl
Innerchr16:61752401..61978860hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38226460
hg19226460
hg18226460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559373
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)nsv1063811
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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