A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041338



Internal ID19130557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13294694..13353796hg38UCSC Ensembl
Innerchr16:13388551..13447653hg19UCSC Ensembl
Innerchr16:13296052..13355154hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3859103
hg1959103
hg1859103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718889
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)nsv1041338
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