A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559366



Internal ID18857647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60499523..60545456hg38UCSC Ensembl
Innerchr16:60533427..60579360hg19UCSC Ensembl
Innerchr16:59090928..59136861hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3845934
hg1945934
hg1845934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067374
Supporting Variants
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)nssv3559366
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