A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046500



Internal ID19135719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19931704..19956028hg38UCSC Ensembl
Innerchr16:19943026..19967350hg19UCSC Ensembl
Innerchr16:19850527..19874851hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3824325
hg1924325
hg1824325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2789n100
Supporting Variantsnssv3542817, nssv3542812, nssv3542824, nssv3542801, nssv3542826, nssv3542822, nssv3542821, nssv3542818, nssv3542823, nssv3542819, nssv3542811, nssv3542797, nssv3542796, nssv3542802, nssv3542814, nssv3542807, nssv3542805, nssv3542810, nssv3542804, nssv3542825, nssv3542827, nssv3542813, nssv3542795, nssv3542820, nssv3542806, nssv3542799, nssv3542828, nssv3542808, nssv3542816, nssv3542815, nssv3542829, nssv3542803, nssv3542798, nssv3542809, nssv3542800
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)nsv1046500
Frequency
Sample Size11257
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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