A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058507



Internal ID19147726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:26525476..26545552hg38UCSC Ensembl
Innerchr16:26536797..26556873hg19UCSC Ensembl
Innerchr16:26444298..26464374hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3820077
hg1920077
hg1820077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549135
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)nsv1058507
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