A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722721



Internal ID19021002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62628255..62687066hg38UCSC Ensembl
Innerchr16:62662159..62720970hg19UCSC Ensembl
Innerchr16:61219660..61278471hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3858812
hg1958812
hg1858812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055410
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)nssv3722721
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