A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568861



Internal ID18867142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42760186..43052691hg38UCSC Ensembl
Innerchr19:43264338..43556843hg19UCSC Ensembl
Innerchr19:47956178..48248683hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38292506
hg19292506
hg18292506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062710
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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