A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044205



Internal ID19133424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7986370..8014271hg38UCSC Ensembl
Innerchr16:8036372..8064273hg19UCSC Ensembl
Innerchr16:7976373..8004274hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3827902
hg1927902
hg1827902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2722n100
Supporting Variantsnssv3557097
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)nsv1044205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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