A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044530



Internal ID19133749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9128386..9209461hg38UCSC Ensembl
Innerchr16:9222243..9303318hg19UCSC Ensembl
Innerchr16:9129744..9210819hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3881076
hg1981076
hg1881076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557117
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)nsv1044530
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