A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066663



Internal ID19155882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42786621..43044850hg38UCSC Ensembl
Innerchr19:43290773..43549002hg19UCSC Ensembl
Innerchr19:47982613..48240842hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38258230
hg19258230
hg18258230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3568999, nssv3568996, nssv3568997, nssv3722904, nssv3568998, nssv3569000, nssv3722903
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066663
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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