A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055277



Internal ID18797808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83643409..83654472hg38UCSC Ensembl
Innerchr16:83677014..83688077hg19UCSC Ensembl
Innerchr16:82234515..82245578hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3811064
hg1911064
hg1811064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559941
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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