A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520889



Internal ID18819170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52042..128355hg38UCSC Ensembl
Innerchr12:161208..237521hg19UCSC Ensembl
Innerchr12:31469..107782hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3876314
hg1976314
hg1876314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050434
Supporting Variants
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520889
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