A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066700



Internal ID19155919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776064..42858488hg38UCSC Ensembl
Innerchr19:43280216..43362640hg19UCSC Ensembl
Innerchr19:47972056..48054480hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3882425
hg1982425
hg1882425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3562n100
Supporting Variantsnssv3568890, nssv3568887, nssv3568894, nssv3722884, nssv3722881, nssv3568895, nssv3568896, nssv3568893, nssv3568885, nssv3568888, nssv3568892, nssv3722883, nssv3568891, nssv3568889, nssv3722882, nssv3722880, nssv3568886
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066700
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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