A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550286



Internal ID18848567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..32644190hg38UCSC Ensembl
Innerchr16:32146874..32655511hg19UCSC Ensembl
Innerchr16:32054375..32563012hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38508638
hg19508638
hg18508638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064674
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550286
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