A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055183



Internal ID19144402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60684885..60934568hg38UCSC Ensembl
Innerchr16:60718789..60968472hg19UCSC Ensembl
Innerchr16:59276290..59525973hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38249684
hg19249684
hg18249684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559368
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)nsv1055183
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer