A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035233



Internal ID18777764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8678512..8730293hg38UCSC Ensembl
Innerchr16:8772369..8824150hg19UCSC Ensembl
Innerchr16:8679870..8731651hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3851782
hg1951782
hg1851782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718869
Samples
Known GenesABAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035233
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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